| Elbs persulfate oxidation | |
|---|---|
| Named after | Karl Elbs |
| Reaction type | Organic redox reaction |
| Identifiers | |
| RSC ontology ID | RXNO:0000179 |
The Elbs persulfate oxidation is the organic reaction of phenols with alkaline potassium persulfate to form para-diphenols.[1]
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Several reviews have been published.[2][3][4]
Reaction mechanism
A reaction mechanism has been postulated which accounts for the observed para substitution featuring the tautomeric para carbanion of the starting phenolate ion:[5] It begins with nucleophilic displacement on the peroxide oxygen of the peroxodisulfate (peroxydisulfate) ion, to give an intermediate sulfate group (3), which is then hydrolyzed to the hydroxyl group.
The reaction is disadvantaged by low chemical yields with recovery of starting material and complete consumption of the persulfate. It is suggested that the phenol in many cases is a catalyst converting the persulfate into a sulfate.
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See also
- Boyland–Sims oxidation
References
- ^ Elbs, K. (1893). "Ueber Nitrohydrochinon". J. Prakt. Chem. (in German). 48: 179–185. doi:10.1002/prac.18930480123.
- ^ Sethna, S. M. (1951). "The Elbs Persulfate Oxidation". Chem. Rev. 49 (1): 91–101. doi:10.1021/cr60152a002.
- ^ Lee, J. B.; Uff, B. C. (1967). "Organic reactions involving electrophilic oxygen". Quart. Rev. 21 (4): 453. doi:10.1039/qr9672100429.
- ^ Behrman, E. J. (1988). "The Persulfate Oxidation of Phenols and Arylamines (The Elbs and the Boyland-Sims Oxidations)". Org. React. 35. pp. 421–511. doi:10.1002/0471264180.or035.02. ISBN 0471264180.
- ^ Behrman, E. J. (2006). "The Elbs and Boyland-Sims peroxydisulfate oxidations". Beilstein Journal of Organic Chemistry. 2 (1): 22. doi:10.1186/1860-5397-2-22. PMC 1697820. PMID 17090305.