Issue 0, 1968

Acylation and alkylation reactions. Part I. The cleavage of benzyl phenyl ethers by aluminium chloride

Abstract

The major products formed by aluminium chloride-catalysed rearrangement of a series of benzyl phenyl ethers in benzene at 5–10° have been shown to be the o-benzylphenol, diphenylmethane, and the phenol.

Article information

Article type
Paper

J. Chem. Soc. B, 1968, 742-744

Acylation and alkylation reactions. Part I. The cleavage of benzyl phenyl ethers by aluminium chloride

M. H. Palmer and G. J. McVie, J. Chem. Soc. B, 1968, 742 DOI: 10.1039/J29680000742

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