Issue 16, 1990

2-Bromomethylprop-2-en-1-yl acetate; synthesis and applications

Abstract

Fluoride-ion-mediated elimination of hydrogen bromide from 3-bromo-2-bromomethylpropyl acetate gave the title compound, the bromine atom of which was specifically substituted by various nucleophiles to yield the corresponding phenyl sulphone, dimethyl malonate, diethylamine, and benzyl sulphide derivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1080-1081

2-Bromomethylprop-2-en-1-yl acetate; synthesis and applications

G. Magnusson and F. Lindqvist, J. Chem. Soc., Chem. Commun., 1990, 1080 DOI: 10.1039/C39900001080

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