Issue 0, 1974

Reaction of bromine with phenyl-substituted tertiary alcohols

Abstract

The reaction between bromine and 1,1-diphenylalkan-1-ols is shown to proceed by dehydration to an alkene, followed in aqueous acetic acid by formation of a bromohydrin which may then rearrange to a ketone. A number of new bromohydrins and bromoalkenes have been prepared.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 135-137

Reaction of bromine with phenyl-substituted tertiary alcohols

D. W. Grant and R. Shilton, J. Chem. Soc., Perkin Trans. 1, 1974, 135 DOI: 10.1039/P19740000135

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