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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965076Generated: October 30, 2026

Water → 3-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1965076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-3-methylbenzonitrileHCID 23160359—
CatalystBenzoyl PeroxideHCID 7187—
SolventAcetonitrileHCID 6342—
Product3-(Bromomethyl)-2-fluorobenzonitrileHCID 6667846570.2%

Reaction Steps

NBS (1.729 g, 9.71 mmol) was added to a solution of 2-fluoro-3-methylbenzonitrile (1.25 g, 9.25 mmol) in acetonitrile (25 mL). The obtained mixture was refluxed, and then benzoic peroxyanhydride (0.045 g, 0.18 mmol) was added. The reaction mixture was refluxed overnight, then cooled to r.t. and water was added. The aqueous phase was discarded and the organic phase was dried over MgSO4 and concentrated. The crude product was purified by flash chromatography using a gradient of EtOAc in heptane as eluent to give the title compound (1.39 g, 70% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 4.75 (s, 2 H) 7.43 (t, 1 H) 7.93 (t, 2 H); MS (EI) m/z 213 M.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415483B2
Source datasetuspto-grants-2013_04
ORD IDord-8d4c778fb0214446a2b25e395497b4a2
Source noteuspto-grants-2013_04