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Cornforth reagent
View on Wikipediafrom Wikipedia
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| Names | |
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| Other names
Pyridinium dichromate
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.039.511 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C10H12N2Cr2O7 | |
| Molar mass | 376.2 g/mol |
| Appearance | orange to brown solid[1] |
| Boiling point | 145 to 147 °C (293 to 297 °F; 418 to 420 K)[1] |
| soluble in water[1] | |
| Hazards | |
| GHS labelling: | |
     
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| Danger | |
| H228, H272, H314, H315, H317, H319, H350, H410 | |
| P201, P202, P210, P220, P221, P240, P241, P260, P261, P264, P272, P273, P280, P281, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P310, P321, P332+P313, P333+P313, P337+P313, P362, P363, P370+P378, P391, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The Cornforth reagent (pyridinium dichromate or PDC) is a pyridinium salt of dichromate with the chemical formula [C5H5NH]2[Cr2O7]. This compound is named after the Australian-British chemist Sir John Warcup Cornforth, who introduced it in 1962.[2][3] The Cornforth reagent is a strong oxidizing agent which can convert primary and secondary alcohols to aldehydes and ketones respectively. In its chemical structure and functions it is closely related to other compounds made from hexavalent chromium oxide, such as pyridinium chlorochromate and Collins reagent. Because of their toxicity, these reagents are rarely used nowadays.[4]
Synthesis and properties
[edit]The Cornforth reagent is prepared by slow addition of a concentrated aqueous solution of chromium trioxide to pyridine. The reaction may cause explosion, which is avoided by thoroughly dissolving the trioxide in water and cooling the solution by ice. The product is filtered, washed with acetone and dried, yielding an orange powder. The powder is stable in air, not particularly hygroscopic and has an almost neutral pH that facilitates its handling; it is only slightly acidic owing to the presence of pyridinium cations. The Cornforth reagent is readily soluble in water, dimethylformamide and dimethyl sulfoxide (DMSO). It is poorly soluble in acetone and chlorinated organic solvents, such as dichloromethane, and forms suspensions.[4][5]
Applications
[edit]The Cornforth reagent is a strong oxidizing agent which can convert primary alcohols to aldehydes and secondary alcohols to ketones, both as a solution or suspension. This application was first mentioned in 1969, but fully developed only in 1979 by E. J. Corey and G. Schmidt. They mentioned that reaction of saturated primary alcohols with PDC, using dimethylformamide as solvent, results in oxidation to carboxylic acids rather than aldehydes. However, no oxidation to carboxylic acids occurs on allylic and benzylic primary alcohols.[6]
The oxidation is usually carried out at ambient conditions, in nearly neutral pH conditions, in dimethylformamide or dichloromethane or their mixture. The choice of solvent or their ratio affects the reaction rate; in particular, higher content of dimethylformamide results in stronger oxidation. The slow oxidation rate for some alcohols can be accelerated by the addition of molecular sieves, organic acids or acetic anhydride or of their combinations. The acceleration by molecular sieves works best when their pore diameter is about 0.3 nm, and it is apparently unrelated to their water absorption capability. Among organic acids, acetic acid, pyridinium trifluoroacetate or pyridinium tosylate can be added, the first one being most efficient and easiest to remove. The achieved acceleration is remarkable, but the reaction inevitably turns from neutral (pH) to acidic. Comparable acceleration is achieved with acetic anhydride, which is used in sugar and nucleoside chemistry. Reaction acceleration depends not only on the additives but also on their form, so all reagents are preferred dry and freshly prepared, and PDC and molecular sieves should be finely ground. The disadvantage of the accelerators is that they may simultaneously promote several oxidation routes thereby reducing the selectivity of the reaction.[4][5]
In its chemical structure and functions, the Cornforth reagent is closely related to other pyridinium salts of hexavalent chromium oxide, such as pyridinium chlorochromate [PyH][CrO3Cl] and to pyridine complexes such as the Collins reagent, CrO3·2Py in dichloromethane and the Sarret reagent, CrO3·2Py in pyridine.[4]
Safety issues
[edit]The Cornforth reagent is very toxic to aquatic life and may cause long-term damage to the environment if released in large amounts. It irritates skin and mucous membranes and may induce allergic reactions; it is carcinogenic. The maximum allowable concentration varies between 0.01 and 0.1 mg·m−3 in air depending on the country. Because it contains hexavalent chromium, it is a suspected carcinogen, and as a strong oxidant, pyridinium dichromate promotes fires, releasing carbon monoxide, carbon dioxide and toxic metal smoke. The fire can be extinguished by water or CO2.[1]
See also
[edit]References
[edit]- ^ a b c d Pyridinium dichromate, MSDS, Alfa Caesar
- ^ Alexander Senning Elsevier's dictionary of chemoetymology: the whies and whences of chemical nomenclature and terminology, Elsevier, 2007, ISBN 0-444-52239-5 p. 94
- ^ Cornforth, R.H.; Cornforth, J.W.; Popjak, G. (1962). "Preparation of R-and S-mevalonolactones". Tetrahedron. 18 (12): 1351–4. doi:10.1016/S0040-4020(01)99289-0.
- ^ a b c d G. Tojo; M. Fernâandez (2006). Oxidation of alcohols to aldehydes and ketones: a guide to current common practice. New York: Springer. pp. 28, 29, 86. ISBN 0-387-23607-4.
- ^ a b Steven V. Ley Oxidation, Elsevier, 1992, ISBN 0-08-040598-3 p. 272
- ^ Corey, E.J.; Schmidt, G. (1979). "Useful procedures for the oxidation of alcohols involving pyridinium dichromate in approtic media". Tetrahedron Lett. 20 (52): 399. doi:10.1016/S0040-4039(01)93515-4.
Cornforth reagent
View on Grokipediafrom Grokipedia
The Cornforth reagent, also known as pyridinium dichromate (PDC), is a chromium(VI)-based oxidizing agent with the molecular formula C10H12Cr2N2O7, utilized in organic synthesis for the selective oxidation of primary alcohols to aldehydes and secondary alcohols to ketones under mild conditions.
This reagent, a dipyridinium salt of dichromic acid, was introduced in 1962 by Australian-British chemist Sir John Warcup Cornforth (Nobel Prize in Chemistry, 1975), along with Rita H. Cornforth and George Popják, during their synthesis of mevalonolactones, where it proved effective for alcohol oxidations without over-oxidation to carboxylic acids.[1] PDC is prepared by adding pyridine to an aqueous solution of chromium trioxide (CrO3), forming an orange crystalline solid that is soluble in water and polar organic solvents like dichloromethane.[2]
Compared to other chromate reagents such as pyridinium chlorochromate (PCC) or the Jones reagent, PDC is notably less acidic and non-hygroscopic, rendering it particularly suitable for oxidizing acid-sensitive substrates while maintaining high selectivity and yields, often at room temperature in aprotic media.[2] Its mechanism involves the formation of a chromate ester intermediate followed by elimination, producing the carbonyl product and reduced chromium species that can be easily removed during workup.[3] Widely adopted since its inception, PDC remains a staple in synthetic laboratories for its stability, commercial availability, and compatibility with a broad range of functional groups, though environmental concerns over chromium waste have prompted exploration of greener alternatives.
Overview
Definition and nomenclature
The Cornforth reagent is a chromium-based oxidizing agent consisting of a pyridinium salt of dichromate, with the chemical formula . It serves as a mild oxidant suitable for use in aqueous or solvent-based systems, particularly for selective oxidations in organic synthesis. The compound has a molar mass of 376.2 g/mol. Named after the Australian-British chemist Sir John Warcup Cornforth, the reagent was introduced in 1962 by J.W. Cornforth, R.H. Cornforth, and G. Popják as part of the synthesis of mevalonolactones.[4] Common synonyms include pyridinium dichromate (PDC) when referring to the isolated salt, though "Cornforth's reagent" specifically denotes the original formulation.[5] The nomenclature distinguishes the original Cornforth reagent—a mixture prepared from chromium trioxide (CrO₃) in pyridine and water, resulting in a hydrated form containing approximately 15% water—from the anhydrous PDC, also known as the Corey-Schmidt reagent, which is the pure, water-free pyridinium dichromate salt isolated for more precise applications.[6] This hydrated nature of the Cornforth variant affects its reactivity, making it less suitable for acid-sensitive substrates compared to the anhydrous PDC.[6]Historical development
The use of pyridinium dichromate (PDC) in aprotic solvents such as dimethylformamide (DMF) was introduced by E. J. Corey and G. Schmidt in 1979 through a seminal publication in Tetrahedron Letters, where it was described as an efficient method for oxidizing primary and secondary alcohols to aldehydes and ketones under aprotic conditions, offering improved selectivity and milder reaction profiles compared to earlier chromium-based oxidants like the Jones reagent.[7] This development built on Corey's prior innovation of pyridinium chlorochromate (PCC) in 1975, which had already advanced the field of controlled alcohol oxidations by minimizing over-oxidation to carboxylic acids.[8] PDC quickly gained traction for its stability as a bright orange solid and ease of preparation by adding pyridine to an aqueous solution of chromium trioxide, enabling practical applications in synthetic organic chemistry. John Warcup Cornforth, who shared the 1975 Nobel Prize in Chemistry with Vladimir Prelog for elucidating the stereochemistry of enzyme-catalyzed reactions, first developed the reagent in 1962 during his studies on lipid and terpene biosynthesis at the Milstead Laboratory of Chemical Enzymology in Sittingbourne, UK. Cornforth's work leveraged the reagent for selective oxidations in complex natural product syntheses, particularly in biosynthetic contexts, where precise control over functional group transformations was essential; his contributions led to the reagent being named the Cornforth reagent in his honor.[6][4] Over time, PDC evolved from its initial aprotic and aqueous formulations to more sustainable variants, reflecting broader trends in green chemistry. Refinements in the 1980s and 1990s optimized its use in dimethylformamide (DMF) for enhanced yields in allylic and benzylic oxidations, while later innovations addressed environmental concerns by developing solvent-free and recoverable systems.Preparation
Synthesis procedure
The standard laboratory preparation of pyridinium dichromate (PDC), the isolated form of the Cornforth reagent, involves dissolving chromium trioxide (CrO₃, 1 equivalent) in water to create an aqueous solution, which is then added dropwise to pyridine (2 equivalents) maintained at 0 °C with vigorous stirring. The addition is continued until the formation of an orange precipitate is complete, after which the mixture is stirred for an additional 30–60 minutes at low temperature. The precipitate is collected by filtration, washed thoroughly with cold acetone to remove excess pyridine and water, and dried under reduced pressure at room temperature. This method yields PDC as a bright orange, crystalline solid suitable for storage and use in subsequent oxidations.[2][6] The product is typically obtained in high yield (80–90%) and can be characterized by infrared spectroscopy, which shows characteristic bands for the dichromate anion, including a Cr=O stretching vibration around 930–950 cm⁻¹, or by elemental analysis confirming the composition [C₅H₅NH]₂[Cr₂O₇].[9] This procedure is suitable for gram-scale preparations but requires careful control of temperature and addition rate to avoid local overheating, which can lead to decomposition of the chromium(VI) species and reduced purity. Excess heat generation is minimized by using an ice bath and slow addition. In the original method reported by Cornforth, the reagent is generated in situ without isolation of PDC by directly mixing chromium trioxide with pyridine and a small amount of water, typically in a 1:2:0.1 molar ratio, and used immediately for alcohol oxidations, particularly to carboxylic acids under aqueous conditions.[6]Variations and related reagents
The Cornforth reagent is typically employed as an in situ aqueous mixture of chromium trioxide, pyridine, and water, generating a hydrated form of pyridinium dichromate (PDC) that incorporates residual water; this hydration reduces selectivity toward allylic alcohols due to potential side reactions involving water.[6] In comparison, PDC itself is isolated as an anhydrous, water-free orange solid, which enhances its compatibility with a wider range of acid-sensitive or water-labile substrates.[2] Modified versions of PDC extend its utility in specific oxidations. For instance, PDC dissolved in dimethylformamide (DMF) promotes the full oxidation of primary alcohols to carboxylic acids, except for allylic variants, by facilitating further reaction of the intermediate aldehyde with trace water under these conditions.[10] Another adaptation, 4-(dimethylamino)pyridinium dichromate (DMAPDC), incorporates a dimethylamino substituent on the pyridine ring to provide milder oxidation conditions suitable for sensitive alcohols.[11] A closely related reagent is pyridinium chlorochromate (PCC, also known as the Corey-Suggs reagent), prepared using hydrochloric acid instead of water to form the chlorochromate anion; this results in greater solubility in nonpolar solvents like dichloromethane and a higher propensity for over-oxidation of primary alcohols to carboxylic acids under moist conditions, unlike the more controlled behavior of PDC. Commercially, PDC is available as the anhydrous solid from suppliers including TCI Chemicals (CAS 20039-37-6), facilitating reproducible use without on-site preparation.[12] The Cornforth mixture, however, is conventionally prepared fresh in the laboratory to maintain activity.[6]Properties
Physical characteristics
The Cornforth reagent, also known as pyridinium dichromate, is typically observed as an orange to brown crystalline solid or powder.[13] This appearance arises from the ionic nature of the compound, which forms stable crystalline structures under ambient conditions.[14] The reagent does not possess a true melting point and instead decomposes upon heating at approximately 145–153 °C.[15] Decomposition occurs over a broader range starting around 177 °C, releasing volatile chromium compounds.[14] It exhibits high solubility in water, reaching up to 943 g/L at 20 °C, and is also readily soluble in polar aprotic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO).[14] In contrast, solubility is limited in less polar solvents like dichloromethane, chloroform, and acetone, and it is insoluble in nonpolar media such as hexane, diethyl ether, and ethyl acetate.[16] The density of the solid is about 1.71 g/cm³ at 20 °C.[17] The compound is hygroscopic, readily absorbing moisture from the air, which can lead to clumping and requires storage under dry, inert conditions to maintain integrity.[14] Spectroscopically, the reagent shows characteristic UV-Vis absorption at 350 nm, attributable to the dichromate anion (Cr₂O₇²⁻), with the solution appearing orange due to this electronic transition.[18] It remains stable in neutral to acidic aqueous media, where this absorbance is prominent.[14]Chemical reactivity
The Cornforth reagent, also known as pyridinium dichromate (PDC), functions as a mild Cr(VI)-based oxidizing agent that exhibits selectivity toward allylic and benzylic alcohols, converting them preferentially to the corresponding aldehydes or ketones due to the enhanced reactivity of these activated substrates.[19] This selectivity arises from the reagent's moderate electrophilicity, which favors hydrogen abstraction at benzylic or allylic positions over saturated alcohols.[2] During oxidation, PDC undergoes stepwise reduction to Cr(III) via a series of electron transfers, typically involving three equivalents of substrate per mole of oxidant to fully reduce the dichromate ion. PDC demonstrates good stability as a bright orange crystalline solid when stored under dry, ambient conditions, remaining viable for several months without significant decomposition. However, it is incompatible with strong bases, which promote decomposition of the Cr(VI) center, and with reducing agents, leading to exothermic reactions or ignition.[20] Its reactivity is influenced by pH, performing optimally in mildly acidic to neutral media (pH 4–7), where the pyridinium counterion maintains a near-neutral environment that minimizes side reactions with acid-labile groups.[2] Reactivity can be modulated by additives; for instance, molecular sieves enhance rates by scavenging trace water, while acetic acid accelerates oxidations through protonation of the dichromate, boosting its electrophilic character.[21] Common side reactions include over-oxidation of primary alcohols to carboxylic acids, particularly in protic or polar aprotic solvents like DMF, where hydration facilitates further reaction. PDC generally remains inert toward isolated alkenes and aromatic rings unless they are activated by adjacent functional groups that direct oxidation.Applications
Alcohol oxidations
The Cornforth reagent, also known as pyridinium dichromate (PDC), is widely employed for the selective oxidation of primary alcohols to aldehydes and secondary alcohols to ketones under mild, aprotic conditions that prevent over-oxidation to carboxylic acids. These reactions typically occur in dichloromethane (CH₂Cl₂) or dimethylformamide (DMF) at room temperature, leveraging the reagent's solubility and stability in such solvents to achieve high selectivity and efficiency. Yields for both primary and secondary alcohol oxidations generally range from 80% to 95%, reflecting the reagent's reliability across a variety of substrates. For primary alcohols, the oxidation proceeds as RCH₂OH → RCHO using 1.5–3 equivalents of the reagent, often with the optional inclusion of 4Å molecular sieves to maintain anhydrous conditions and minimize hydration of the intermediate aldehyde. Reaction times range from 1 to 24 hours, after which the mixture is worked up by extraction with diethyl ether followed by treatment with aqueous sodium bisulfite (NaHSO₃) to reduce excess Cr(VI) species and remove chromium residues. This protocol ensures clean isolation of the aldehyde product without further oxidation. A representative example is the conversion of the allylic primary alcohol geraniol to geranial, which affords the α,β-unsaturated aldehyde in approximately 86% yield while preserving the trans double bond configuration.[22] Secondary alcohols are oxidized to ketones (R₂CHOH → R₂C=O) under analogous conditions, exhibiting high selectivity even in the presence of other functional groups. The same 1.5–3 equivalents of reagent, solvent, and workup procedure apply, with reaction times similarly spanning 1–24 hours at room temperature. This transformation is particularly useful for complex molecules.Other synthetic uses
The Cornforth reagent, or pyridinium dichromate (PDC), facilitates selective oxidation of allylic alcohols to the corresponding α,β-unsaturated carbonyl compounds in non-aqueous media, preventing isomerization of the double bond and preserving stereochemistry. This process is particularly effective in dichloromethane at room temperature under anhydrous conditions, allowing oxidation in the presence of other alcohol functionalities without over-oxidation.[6] PDC also enables mild oxidation of sulfides to sulfoxides, such as the conversion of alkyl aryl sulfides in acetonitrile, proceeding via a radical mechanism for certain substrates and yielding the products without significant over-oxidation to sulfones. Typical yields for such transformations range from 70-90%, depending on the substrate, with electron-withdrawing groups on aryl sulfides moderately reducing reactivity.[23] In combined systems, PDC with sodium nitrite (NaNO₂) promotes nitration of aromatic and heteroaromatic compounds under acid-free conditions in aqueous acetonitrile, generating nitro derivatives efficiently via an electrophilic mechanism involving a nitrating intermediate. This approach achieves high yields, especially under microwave assistance (4-6 minutes reaction time), offering a practical route to nitroarenes from electron-rich substrates like phenols.[25] PDC has found application in polymer chemistry for selective side-chain modifications, such as oxidation of pendant alcohol groups in polyols, enabling controlled functionalization while maintaining polymer integrity.[26] Post-2000 developments include PDC's continued role in total syntheses of natural product intermediates, providing mild oxidation steps compatible with sensitive scaffolds.[3]Reaction mechanism
General pathway
The oxidation of alcohols using the Cornforth reagent, pyridinium dichromate (PDC), proceeds through a multi-step pathway typical of Cr(VI)-based oxidants. The initial step involves the nucleophilic attack by the oxygen atom of the alcohol on the electrophilic chromium(VI) center, leading to the formation of a chromate ester intermediate (R-O-CrO₂(OH)). This coordination facilitates the activation of the alcohol for subsequent oxidation.[27] Following ester formation, the pathway continues with an oxidative elimination step, where a base (such as pyridine from the reagent) abstracts an alpha-hydrogen from the oxygen-bound carbon. This alpha-hydride elimination generates the carbonyl product (aldehyde from primary alcohols or ketone from secondary alcohols) and reduces the chromium to the Cr(IV) state. The Cr(IV) species is then further reduced to Cr(III) through additional interactions, often involving disproportionation or reaction with another alcohol molecule, completing the overall reduction of the oxidant.[27][3] The overall stoichiometry for the oxidation of three alcohol molecules by one equivalent of dichromate ion reflects the two-electron transfer per alcohol to form the carbonyl compound: This balanced equation accounts for the net reduction of two Cr(VI) centers to Cr(III) while oxidizing the alcohols.[27] Solvent choice significantly influences the pathway's outcome, particularly for primary alcohols. In dichloromethane (DCM), the reaction typically halts at the aldehyde stage due to the non-aqueous conditions that limit hydration and further oxidation. In contrast, polar solvents like dimethylformamide (DMF) or aqueous media promote hydration of the aldehyde intermediate, allowing progression to the carboxylic acid.[28]Key intermediates
The key intermediates in the mechanism of the Cornforth reagent, or pyridinium dichromate (PDC), involve transient chromium species that facilitate the oxidation of alcohols. The initial adduct is a chromate ester formed by the coordination of the alcohol to the chromium(VI) center, represented as [\ce{PyH+}][(\ce{RO})CrO3Py}-], where Py denotes pyridine and R is the alkyl group from the alcohol.[3] This ester arises from nucleophilic attack by the alcohol oxygen on the electrophilic Cr(VI), displacing a ligand or equilibrating with the dichromate structure. Following ester formation, the mechanism proceeds through elimination, generating a Cr(IV) oxo species as a gem-diol-like intermediate prior to further reduction. This Cr(IV) intermediate, often formulated as a hydrated oxo complex such as , results from the alpha-hydride shift and breakage of the C-O bond in the ester, transferring two electrons to reduce Cr(VI) to Cr(IV).[29] EPR spectroscopy provides evidence for Cr(IV) in reaction mixtures of Cr(VI)-based alcohol oxidations, detecting paramagnetic d² signals attributable to this oxo species, which persists briefly before reacting with additional Cr(VI) or substrate.[29] The gem-diol character arises from coordination of water or solvent to the reduced chromium, stabilizing the intermediate and influencing subsequent reductions to Cr(III). Pyridine plays a crucial role in stabilizing the Cr(VI) species by acting as a neutral ligand, coordinating to the metal center to form soluble pyridinium complexes that prevent precipitation of insoluble chromates in organic media like DMF.[6] This ligation moderates the acidity compared to anhydrous variants and enhances selectivity for carbonyl formation. In the Cornforth variant, which incorporates water during preparation, hydration of the Cr(VI) center alters the coordination sphere, promoting over-oxidation of aldehydes to carboxylic acids by facilitating gem-diol formation on the product, thus reducing selectivity for aldehydes from primary alcohols.[6] Isotope labeling studies support the involvement of these intermediates, particularly confirming the rate-determining hydride transfer from the chromate ester. Oxidation of [1,1-²H₂]ethanol by PDC in DMSO exhibits a primary deuterium kinetic isotope effect of at 298 K, indicating cleavage of the α-C-H bond in the slow step and consistent with a concerted cyclic transition state leading to the Cr(IV) oxo species.[30] This effect underscores the ester's role as the precursor to elimination, with values ranging from 5.1 to 6.0 across 288–318 K, aligning with hydride-ion transfer mechanisms in Cr(VI) oxidations.[30]Safety and handling
Health hazards
The Cornforth reagent, or pyridinium dichromate, contains hexavalent chromium (Cr(VI)), which is classified as a Group 1 carcinogen to humans by the International Agency for Research on Cancer (IARC), primarily due to its association with lung cancer from occupational exposures.[31] Cr(VI) compounds exhibit acute oral toxicity in rats with an LD50 of approximately 50–150 mg/kg body weight.[32] Chronic exposure can lead to respiratory tract irritation, including nasal septum perforation and chrome ulcers (skin lesions resembling holes) from direct contact.[33] Exposure to the reagent occurs primarily through inhalation of dust or aerosols, which is the most significant route in laboratory settings and can result in lung cancer and other respiratory diseases, as evidenced by epidemiological studies of Cr(VI)-exposed workers.[34] Skin contact causes severe dermatitis, allergic reactions, and burns due to its corrosive nature, while ingestion leads to gastrointestinal hemorrhage, nausea, and vomiting from acute mucosal damage.[33] Ocular exposure results in immediate irritation and potential corneal damage.[35] At the cellular level, chronic effects involve DNA damage through the generation of reactive oxygen species (ROS), contributing to genotoxicity and oncogenesis, particularly in the respiratory epithelium.[36] Acute symptoms include eye and skin irritation, along with systemic nausea from any exposure route.[37] Regulatory standards limit occupational exposure to Cr(VI) to a permissible exposure limit (PEL) of 5 µg/m³ (0.005 mg/m³) as an 8-hour time-weighted average, enforced by the Occupational Safety and Health Administration (OSHA).[38] Safe handling requires personal protective equipment, including gloves, eye protection, and respiratory safeguards, with operations conducted in a fume hood to minimize inhalation risks. As a solid reagent, PDC requires additional precautions to avoid generating inhalable dust.[37]Environmental considerations
The Cornforth reagent, a chromium(VI)-based oxidant, contributes to environmental pollution primarily through the release of hexavalent chromium (Cr(VI)), which is highly mobile in aqueous environments due to its solubility and stability under neutral to alkaline conditions. This mobility allows Cr(VI) to leach into surface and groundwater, posing risks to ecosystems. Cr(VI) is acutely toxic to aquatic organisms, with 96-hour LC50 values as low as 0.067 mg/L for freshwater invertebrates such as the scud (Gammarus pseudolimnaeus) and approximately 17 mg/L for fish like the fathead minnow (Pimephales promelas); toxicity decreases with increasing water hardness but remains significant in soft waters.[39] In soils, Cr(VI) exhibits persistence, resisting adsorption and facilitating long-term contamination of groundwater aquifers, as soluble forms do not readily precipitate or degrade.[40] Reactions employing the Cornforth reagent generate substantial hazardous waste, primarily in the form of reduced Cr(III) sludge, which requires specialized treatment and disposal to prevent further environmental release. Stoichiometric use of the reagent—typically 1.5–2 equivalents per mole of alcohol—results in significant solid waste, estimated at several hundred grams of chromium-containing residue per mole of product in laboratory-scale oxidations, complicating waste management and increasing disposal costs. This Cr(III) sludge, while less toxic than Cr(VI), can still mobilize under acidic conditions and contribute to sediment accumulation in water bodies.[41] Efforts in green chemistry have promoted alternatives to chromium-based oxidants like the Cornforth reagent to mitigate these impacts, favoring non-metal systems that reduce or eliminate heavy metal waste. For instance, TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) serves as a catalytic mediator with co-oxidants like bleach, enabling efficient alcohol oxidations with minimal waste and recyclable components. Similarly, IBX (2-iodoxybenzoic acid) offers a stoichiometric organic hypervalent iodine oxidant that produces benign byproducts like iodic acid, which can be recycled, though it requires careful handling of iodine residues.[42] Recycling strategies for chromium from reaction waste, such as re-oxidation of Cr(III) to Cr(VI), have been explored but prove inefficient due to energy demands and challenges in laboratory settings.[43] Regulatory frameworks address Cr(VI) risks from reagents like the Cornforth variant, classifying it as a hazardous substance. The U.S. Environmental Protection Agency (EPA) designates Cr(VI) compounds as known human carcinogens and probable carcinogens via ingestion, with strict effluent guidelines limiting discharges to protect aquatic life. Under the European Union's REACH regulation (Annex XVII, entry 72), Cr(VI) is restricted in consumer products such as leather articles to below 3 mg/kg to prevent migration into the environment. Recent studies in the 2020s have advanced sustainable mimics, including bio-derived organocatalysts that replicate chromium oxidation selectivity without metal toxicity, supporting a transition to biodegradable or recyclable systems.[44]References
- https://www.[researchgate](/page/ResearchGate).net/publication/352731928_Studies_on_the_Oxidation_of_some_Sulfides_with_Pyridinium_Dichromate_in_Acetonitrile_medium