Issue 0, 1984

Attempted synthesis of (9Z)-methyl 12-hydroperoxyoctadec-9-enoate

Abstract

The silver trifluoroacetate-assisted reaction of alkyl halides with hydrogen peroxide has been investigated. Methyl 12-bromostearate furnished, for the first time, methyl 12-hydroperoxystearate in 34% yield. Methyl 12-bromo-oleate, however, gave cyclopropane hydroperoxides (via a homoallylic cation rearrangement) and hydroperoxy epidioxides (presumably via methyl 12-hydroperoxyoleate which could not be isolated). Methyl 9-t-butylperoxy-10,11-methyleneheptadecanoate was produced by the reaction of methyl 12-bromo-oleate with t-butyl hydroperoxide in the presence of silver trifluoroacetate. None of these transformations occurred when silver trifluoroacetate was replaced by the acetate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 2217-2220

Attempted synthesis of (9Z)-methyl 12-hydroperoxyoctadec-9-enoate

E. Bascetta and F. D. Gunstone, J. Chem. Soc., Perkin Trans. 1, 1984, 2217 DOI: 10.1039/P19840002217

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