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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657344Generated: October 25, 2026

N-bromobutanimide → 3-Bromo-5-(bromomethyl)benzonitrile

https://huagongshe.com/reaction/657344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Bromo-5-methylbenzonitrileHCID 14567858—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-5-(bromomethyl)benzonitrileHCID 14567861101%

Reaction Steps

A mixture of 3-bromo-5-methylbenzonitrile (9.80 g, 45.0 mmol), NBS (8.90 g, 45.0 mmol) and BPO (0.40 g) in CCl4 (250 mL) was heated for 10 h at reflux. The reaction mixture was cooled to room temperature and filtered, and the organic phase was washed successively with saturated sodium bicarbonate (100 mL), water (2×50 mL) and brine (2×50 mL). The combined organic phases were dried over Na2SO4 and concentrated in vacuum to give 12.5 g of crude 3-bromo-5-(bromomethyl)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-cd5557a76e354b5fab55d9b9ce7f7aa9
Source noteuspto-grants-2011_12