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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543870Generated: November 1, 2026

p-Bromoacetophenone → 1-Bromo-4-(prop-1-en-2-yl)benzene

https://huagongshe.com/reaction/543870

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantTriphenylmethyl phosphonium bromideHCID 21951224—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-Bromo-4-(prop-1-en-2-yl)benzeneHCID 361441058.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a slurry of triphenylmethylphosphonium bromide (71.4 g, 200 mmole), in 500 ml dry THF at 0° C., were slowly added dropwise 135 ml (200 mmole) 1.44 M n-butyllithium in hexane. The mixture was stirred 30 minutes at 0° C., and a solution of 39.8 g (200 mmole) p-bromoacetophenone, in 100 ml dry THF, was slowly added dropwise. The mixture was allowed to warm slowly to ambient temperature, whereafter stirring was continued overnight. The stirred mixture was next filtered and the solvent removed by careful distillation at atmospheric pressure, the resulting residue was diluted with hexane, filtered, and the hexane removed by distillation. The remaining material was distilled, using a water aspirator vacuum, to produce 23.2 g (58.3% yield) of p-bromo-α-methylstyrene, bp 95°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04447542
Source datasetuspto-grants-1984_05
ORD IDord-2fd29c4ecfc743fc98fae64721d15d67
Source noteuspto-grants-1984_05