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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453438Generated: October 30, 2026

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

https://huagongshe.com/reaction/453438

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 numberUS08492430B2
Source datasetuspto-grants-2013_07
ORD IDord-9fc64eb507bc45d3baf8be19f2f026f4
Source noteuspto-grants-2013_07