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.
Please wait while we load your content...