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Issue 16, 1990
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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.

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Article information


J. Chem. Soc., Chem. Commun., 1990, 1080-1081
Article type
Paper

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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