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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705799Generated: October 30, 2026

Water → 3-(3-Bromo-4-fluorophenyl)propanenitrile

https://huagongshe.com/reaction/705799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-3-(3-Bromo-4-fluorophenyl)acrylonitrileHCID 61702072—
SolventEthanolHCID 702—
Product3-(3-Bromo-4-fluorophenyl)propanenitrileHCID 5343430181.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of (E)-3-(3-bromo-4-fluorophenyl)acrylonitrile (35.0 g, 108 mmol) in ethanol (20 mL) at 0° C. was added sodium tetrahydroborate (16.40 g, 434 mmol). The reaction mixture was allowed to warm to 70° C. and stirred for 4 h. Water was added to quench the reaction, and the organic layer was separated. The water layer was extracted with DCM twice, and the combined organic phase was dried and concentrated. The residue was purified by chromatography to afford the title compound as an oil (20 g, 64.7% yield). LCMS: rt=1.45 min, [M+H+]=228

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-7bae86022e174a06989fd226a8c83e4e
Source noteuspto-grants-2015_11