Abstract
Bromination of alkenes has been conducted in a room temperature ionic liquid {[bmim]+ CCl3COO– (1–butyl–3–methylimidazolium trichloroacetate)} involving the oxidation of NaBr by hydrogen peroxide with no catalyst. Comparatively fast reactions, good yields and the atom economic nature make this environmentally benign reaction an appealing procedure for alkene and alkyne bromination.
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