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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770922Generated: October 31, 2026

Water → 3-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1770922

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, 2H) 7.43 (t, 1H) 7.93 (t, 2H); MS (EI) m/z 213 M+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248129B2
Source datasetuspto-grants-2016_02
ORD IDord-91876803bc8b42a2b000d75e113a2814
Source noteuspto-grants-2016_02