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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627250Generated: November 3, 2026

Water → 5-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1627250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-5-methylbenzonitrileHCID 2774584—
SolventCarbon TetrachlorideHCID 5943—
Product5-(Bromomethyl)-2-fluorobenzonitrileHCID 277393133.6%

Reaction Steps

A solution of 2-fluoro-5-methylbenzonitrile (3.00 g, 22 mmol), N-bromosuccinimide (4.12 g, 23 mmol) and benzoyl peroxide (1.07 g, 4.4 mmol) in CCl4 (100 mL) was heated at reflux 6 h. The reaction mixture was cooled to room temperature and then combined with water. The separated organic phase was dried over MgSO4, filtered through a Celite™ pad, and evaporated under reduced pressure. Purification by flash chromatography (Hex/EtOAc, 20:1) gave 5-(bromomethyl)-2-fluorobenzonitrile (1.58 g, 33% yield) as an oil. 1H NMR (CDCl3, 400 MHz): δ 4.45 (s, 2H), 7.21 (m, 1H), 7.65 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785488B2
Source datasetuspto-grants-2014_07
ORD IDord-3df850d2a6d04bf8bbda0420d070fd5e
Source noteuspto-grants-2014_07