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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787131Generated: October 31, 2026

Cumene → 2-Bromo-1-(4-(propan-2-yl)phenyl)ethan-1-one

https://huagongshe.com/reaction/1787131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCumeneHCID 7406—
ReactantBromoacetyl bromideHCID 61147—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(4-(propan-2-yl)phenyl)ethan-1-oneHCID 14042756—

Reaction Steps

To a solution of cumene (27.8 mL, 200 mmol) and aluminum chloride (32.0 g, 240 mmol) in dichloromethane (300 mL) was added bromoacetylbromide (19.1 mL, 220 mmol) at −10° C., and the mixture was stirred at the same temperature for 2 hours. The reaction solution was poured into ice-cold water, and an organic layer was separated. The organic layer was washed with a saturated sodium hydrogen carbonate solution and a saturated brine, and then was dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9) to obtain 2-bromo-1-(4-isopropylphenyl)ethanone of oily matter. The obtained oily matter was added to a solution of 3,5-dimethylphenol (29.3 g, 240 mmol) and potassium carbonate (33.2 g, 240 mmol) in acetone (500 mL), and the mixture then was stirred under heat and reflux for 12 hours. The reaction solution was ice-cooled and poured into cold water, which was extracted with diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507841B2
Source datasetuspto-grants-2009_03
ORD IDord-bdfdb7fc84a14927a0d813fd6345543c
Source noteuspto-grants-2009_03