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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322562Generated: October 31, 2026

N-bromobutanimide → 2-(Bromomethyl)-5-fluorobenzonitrile

https://huagongshe.com/reaction/322562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Fluoro-2-methylbenzonitrileHCID 522668—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-5-fluorobenzonitrileHCID 22015770102%

Reaction Steps

A mixture of 5-fluoro-2-methylbenzonitrile (10.0 g, 74.0 mmol), N-bromosuccinimide (NMS, 13.2 g, 74.0 mmol), benzoyl peroxide (0.2 g, 0.82 mmol), and carbon tetrachloride (100 mL) was refluxed for 18 h. The reaction mixture was then cooled to room temperature and filtered through fritted glass. The solid in the funnel was washed with carbon tetrachloride (3×50 mL) and evaporated to dryness under vacuum to provide 16.1 g, 102% yield of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211245B1
Source datasetuspto-grants-2001_04
ORD IDord-8a85bffe9d414d689a276bf274601bbe
Source noteuspto-grants-2001_04