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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500509Generated: November 3, 2026

p-Bromoacetophenone → 4-Bromophenacyl bromide

https://huagongshe.com/reaction/1500509

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantBromineHCID 24408—
SolventDichloromethaneHCID 6344—
Product4-Bromophenacyl bromideHCID 745486.3%

Reaction Steps

Bromine (80 g, 500 mmol) was added dropwise to a solution of 1-(4-bromo-phenyl)-ethanone (100 g, 500 mmol) in dichloromethane (1500 mL) at ambient temperature. The reaction mixture was stirred for 3 h and then concentrated. The residue was washed with dichloromethane (100 mL) to give the crude title compound (120 g, 86% yield) as a white solid. 1H NMR (CDCl3, 400 MHz) δ (ppm): 7.78 (d, J=8.4 Hz, 2H), 7.57 (d, J=8.4 Hz, 2H), 4.32 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206159B2
Source datasetuspto-grants-2015_12
ORD IDord-9ff7908dfa2e4bbabf947f07f0d3a9b4
Source noteuspto-grants-2015_12