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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861428Generated: October 30, 2026

Allyl bromide → 4-(ALLYLOXY)BENZONITRILE

https://huagongshe.com/reaction/861428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant4-CyanophenolHCID 13019—
SolventAcetoneHCID 180—
Product4-(ALLYLOXY)BENZONITRILEHCID 257949—

Reaction Steps

A solution of 4-cyanophenol (50 g), allyl bromide (27.2 ml) potassium carbonate (47.8 g) in acetone (100 ml) was heated at reflux for 16 hours. The reaction mixture was evaporated, water was added to the residue and the aqueous mixture was extracted with diethyl ether. The diethyl ether extract was washed with dilute aqueous sodium hydroxide solution, dried (MgSO4) and evaporated to give 4-cyanophenyl allyl ether as a solid, m.p. 41.6° C.; microanalysis, found: C 75.1; H, 5.8; N, 8.7%; C10H9NO2 requires: C, 75.5; H, 5.7; N, 8.8%; NMR: 4.55-4.65(2H,m), 5.2-5.4(2H,m), 5.9-6.05(1H,m), 7.0-7.1(2H,m) and 7.65-7.75(2H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714496
Source datasetuspto-grants-1998_02
ORD IDord-db7bd92a30094e198e7714cced1fed7f
Source noteuspto-grants-1998_02