Issue 3, 1980

meta-Bromination of phenols in superacids

Abstract

In SbF5–HF, para-alkylated or 2,6-dialkylated phenols (and their ethers) react with bromine to give the corresponding meta-bromo-substituted compounds; the mechanism implies bromination of the O-protonated substrate.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 110-111

meta-Bromination of phenols in superacids

J. Jacquesy, M. Jouannetaud and S. Makani, J. Chem. Soc., Chem. Commun., 1980, 110 DOI: 10.1039/C39800000110

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