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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908892Generated: October 27, 2026

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

https://huagongshe.com/reaction/1908892

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 numberUS08598226B2
Source datasetuspto-grants-2013_12
ORD IDord-5d39b46c408a4bb3b73cf782c7cbd8a2
Source noteuspto-grants-2013_12