Reactions of Some Tocopherols with the Methyl Radical

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Abstract
The reactivity of some tocopherols (vitamin E) with the methyl radical was examined. When the methyl radical was generated from dimethyl sulfoxide by the action of H2O2 in the presence of ferrous sulfate, either .beta.-tocopherol or .gamma.-tocopherol reacted with it to give the corresponding methyl ether and 2,5,5,7,8-pentamethyl-2-(4,8,12-trimethyltridecyl)chroman-6(5H)-one in low yields. Tocol afforded only a small amount of its methyl ether. 5,7-Dimethyltocol was converted to its methyl ether and 2,5,5,7-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6(5H)-one in 9 and 38% yields, respectively. Taken with the previous data on .alpha.-tocopherol, these results indicate that the radical scavenging abilities of tocopherols against the methyl radical are in the following order: .alpha.-tocopherol .gtoreq. 5,7-dimethyltocol .beta.-tocopherol = .gamma.-tocopherol .gtoreq. tocol.
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