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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15649Generated: October 31, 2026

N-bromobutanimide → 4-Bromo-3-(bromomethyl)-5-methylphenyl acetate

https://huagongshe.com/reaction/15649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Bromo-3,5-dimethylphenyl acetateHCID 15184685—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-3-(bromomethyl)-5-methylphenyl acetateHCID 1518468673%

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of 4-bromo-3,5-dimethylphenyl acetate (12.1 g, 49.8 mmol), N-bromosuccinimide (9.79 g, 55.0 mmol) and 2,2′-azobisisobutyronitrile (82.1 mg, 0.500 mmol) in carbon tetrachloride (100 mL) was stirred at 75° C. for 5 hr under nitrogen atmosphere. The reaction mixture was ice-cooled, and concentrated under reduced pressure. The residue was diluted with diethyl ether, the insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was-purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75) to give the title compound (11.7 g, yield 73%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732626B2
Source datasetuspto-grants-2010_06
ORD IDord-6bd7035410354fee829adc3e25217709
Source noteuspto-grants-2010_06