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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657319Generated: October 27, 2026

N-bromobutanimide → 2-Bromo-4-(bromomethyl)benzonitrile

https://huagongshe.com/reaction/657319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-4-methylbenzonitrileHCID 820802—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-4-(bromomethyl)benzonitrileHCID 53425521100%

Reaction Steps

A mixture of 2-bromo-4-methylbenzonitrile (13.3 g, 81.4 mmol), NBS (14.4 g, 84.4 mmol) and BPO (0.20 g) in CCl4 (150 mL) was heated for 4 h at reflux. The reaction mixture was cooled to room temperature and filtered. Then the solid was washed with CCl4 (20 mL×2) and the combined filtrates were washed successively with saturated sodium bicarbonate (50 mL), water (2×100 mL) and sodium thiosulfate (50 mL). The organic phase was dried over NaSO4 and concentrated in vacuum afforded the titled compound, 2-bromo-4-(bromomethyl)benzonitrile (18.7 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-32141e78755e4bf5b591b9e2156da638
Source noteuspto-grants-2011_12