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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107063Generated: October 26, 2026

p-Bromochlorobenzene → 1-Allyl-4-chlorobenzene

https://huagongshe.com/reaction/2107063

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product1-Allyl-4-chlorobenzeneHCID 11019064—

Reaction Steps

To a suspension of magnesium turnings (9.6 g) in anhydrous ether (50 ml) was added dropwise to a solution of p-chlorobromobenzene (76.6 g) in anhydrous ether (500 ml) at such a rate as to maintain reflux. After refluxing for a further 20 minutes, the solution was cooled to 5o and a solution of allyl bromide (48.4 g) in anhydrous ether (100 ml) was added over 15 minutes. After 30 minutes the solution was allowed to warm to room temperature, and then saturated ammonium chloride was added dropwise, cautiously to avoid excessive frothing. The organic layer was separated and the aqueous phase was extracted with ether. After washing the ether extracts with water and drying, evaporation of the solvent gave a pale yellow oil which was purified by fractional distillation to give 3-(4-chlorophenyl)prop-1-ene as a colourless oil, b.p. 72°-74°/4 mm Hg. (532 Pa).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933357
Source datasetuspto-grants-1990_06
ORD IDord-8f051d5146a3433f82cc5b85d57b93ba
Source noteuspto-grants-1990_06