Swern oxidation
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Swern_oxidation".

The Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine.[1][2][3] The reaction is known for its mild character and wide tolerance of functional groups.[4][5][6][7]

The Swern oxidation.

The by-products are dimethyl sulfide (Me2S), carbon monoxide (CO), carbon dioxide (CO2) and — when triethylamine is used as base — triethylammonium chloride (Et3NHCl). Two of the by-products, dimethyl sulfide and carbon monoxide, are very toxic volatile compounds, so the reaction and the work-up needs to be performed in a fume hood. Dimethyl sulfide is a volatile liquid (B.P. 37 °C) with an unpleasant odour. A convenient way to reduce the stench of dimethyl sulfide is to treat the crude product mixture with oxone, whereupon the sulfide is converted to dimethyl sulfoxide, which has no odor.

Several reviews have been published.[8][9][10]

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Mechanism

The first step of the Swern oxidation is the low-temperature reaction of dimethyl sulfoxide (DMSO), 1a & 1b, with oxalyl chloride, 2. The first intermediate, 3, quickly decomposes giving off CO2 and CO and producing dimethylchlorosulfonium chloride, 4.

Dimethylchlorosulfonium chloride formation.

After addition of the alcohol 5, the dimethylchlorosulfonium chloride 4 reacts with the alcohol to give the key alkoxysulfonium ion intermediate, 6. The addition of at least 2 equivalents of base — typically triethylamine — will deprotonate the alkoxysulfonium ion to give the sulfur ylide 7. In a five-membered ring transition state, the sulfur ylide 7 decomposes to give dimethyl sulfide and the desired ketone (or aldehyde) 8.

The mechanism of the Swern oxidation.

Variations

When using oxalyl chloride as the dehydration agent, the reaction must be kept colder than -60 °C to avoid side reactions. With trifluoroacetic anhydride instead of oxalyl chloride, the reaction can be warmed to -30 °C without side reactions. Other methods for the activation of DMSO to initiate the formation of the key intermediate 6 are the use of carbodiimides (Pfitzner-Moffatt oxidation) and pyridine-sulfur trioxide complex (Parikh-Doering oxidation).

In some cases, the use of triethylamine as the base can lead to epimerisation at the carbon alpha to the newly formed carbonyl. Using the bulkier base diisopropylethylamine (i-Pr2NEt, Hünig's base) can mitigate this side reaction.

Considerations

Dimethyl sulfide, a byproduct of the Swern oxidation, is one of the most foul odors known in organic chemistry. Human olfactory glands can detect this compound in concentrations as low as parts per billion. A simple remedy for this bothersome problem is to rinse used glassware with bleach (usually containing sodium hypochlorite), which will oxidize the dimethyl sulfide, eliminating the smell.

See also

References

  1. ^ Kanji Omura and Daniel Swern (1978). "Oxidation of alcohols by “activated” dimethyl sulfoxide. a preparative, steric and mechanistic study". Tetrahedron 34: 1651. doi:10.1016/0040-4020(78)80197-5. )
  2. ^ A. J. Mancuso, D. S. Brownfain and D. Swern (1979). "Structure of the dimethyl sulfoxide-oxalyl chloride reaction product. Oxidation of heteroaromatic and diverse alcohols to carbonyl compounds". J. Org. Chem. 44 (23): 4148–4150. doi:10.1021/jo01337a028. 
  3. ^ A. J. Mancuso, S.-L. Huang and D. Swern (1978). "Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride". J. Org. Chem. 43 (12): 2480–2482. doi:10.1021/jo00406a041. 
  4. ^ Dondoni, A.; Perrone, D. (2004). "Synthesis of 1,1-Dimethyl Ethyl-(S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate by Oxidation of the Alcohol". Org. Synth.; Coll. Vol. 10: 320. 
  5. ^ Bishop, R. (1998). "9-Thiabicyclo[3.3.1]nonane-2,6-dione". Org. Synth.; Coll. Vol. 9: 692. 
  6. ^ Leopold, E. J. (1990). "Selective Hydroboration of a 1,3,7-Triene: Homogeraniol". Org. Synth.; Coll. Vol. 7: 258. 
  7. ^ Gabriel Tojo and Marcos Fernández (2006). Oxidation of Alcohols to Aldehydes and Ketones: A Guide to Current Common Practice. Springer. ISBN 0387236074. 
  8. ^ Mancuso, A. J.; Swern, D. (1981). "Activated Dimethyl Sulfoxide: Useful Reagents for Synthesis" (Review). Synthesis 1981: 165–185. doi:10.1055/s-1981-29377. 
  9. ^ Tidwell, T. T. (1990). "Oxidation of Alcohols to Carbonyl Compounds via Alkoxysulfonium Ylides: The Moffatt, Swern, and Related Oxidations" (Review). Org. React. 39: 297–572. doi:10.1002/0471264180.or039.03. 
  10. ^ Tidwell, T. T. (1990). "Oxidation of Alcohols by Activated Dimethyl Sulfoxide and Related Reactions: An Update" (Review). Synthesis 1990: 857–870. doi:10.1055/s-1990-27036. 

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