Issue 23, 1985

A convenient synthesis of o-methylbenzylamine derivatives from benzyl halides: the improved Sommelet–Hauser rearrangement

Abstract

Desilylation by fluoride anion of benzyldimethyl(trimethylsilylmethyl)ammonium halides having a Cl, CN, or AcO substituent on the benzene ring gave high yields of the Sommelet–Hauser rearrangement products at room temperature.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1684-1685

A convenient synthesis of o-methylbenzylamine derivatives from benzyl halides: the improved Sommelet–Hauser rearrangement

M. Nakano and Y. Sato, J. Chem. Soc., Chem. Commun., 1985, 1684 DOI: 10.1039/C39850001684

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