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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231671Generated: October 31, 2026

Allyl bromide → 4-(ALLYLOXY)BENZONITRILE

https://huagongshe.com/reaction/2231671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-CyanophenolHCID 13019—
SolventAcetoneHCID 180—
Product4-(ALLYLOXY)BENZONITRILEHCID 25794996%

Reaction Steps

A mixture comprising 29.75 g of 4-cyanophenol, 33.27 g of allyl bromide, 41.46 g of potassium carbonate and 350 ml of acetone, was refluxed under stirring for 4 hours. Acetone was distilled, and water was added to the residue. The mixture was extracted with benzene. The benzene layer was washed sequentially with a 5% sodium hydroxide aqueous solution and water, and dried over sodium sulfate. Then, the solvent was distilled off to obtain a pale yellow oily substance. The residual substance was crystallized from n-hexane-ethyl ether to obtain 38.16 g of 4-allyloxy benzonitrile as colorless crystals having a melting point of from 40.5° to 41° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783462
Source datasetuspto-grants-1988_11
ORD IDord-394c0f2782b044788ba171e7aa87b880
Source noteuspto-grants-1988_11