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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855268Generated: October 28, 2026

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

https://huagongshe.com/reaction/855268

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantPhosphine, triphenyl-, hydrobromideHCID 517696—
ReactantButyllithiumHCID 178418339—
SolventDimethyl SulfoxideHCID 679—
Product1-Bromo-4-(prop-1-en-2-yl)benzeneHCID 361441053%

Reaction Steps

To a solution of triphenylphosphonium bromide (17.94 g, 50.24 mmol) in DMSO (10 ml) was added n-BuLi (39.25 ml, 1.6M solution in hexane, 62.80 mmol). The solution was stirred at rt for 1 h and to this was added a solution of 4-bromoacetophenone (10.00 g, 50.24 mmol) in DMSO (4 ml). The reaction mixture was then stirred at rt overnight and then quenched with water and the product was extracted with pentane. The organic layers were combined washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by filtration through a short pad of silica using pentane as eluant to give 1-bromo-4-isopropenylbenzene (5.23 g, 53%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ 7.45 (d, J=9.0 Hz, 2H), 7.32 (d, J=9.0 Hz, 2H), 5.36 (m, 1H), 5.10 (m, 1H), 2.12 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-79570d942cfa40f5aed0615cfbfef6d1
Source noteuspto-grants-2007_08