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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474554Generated: October 31, 2026

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

https://huagongshe.com/reaction/474554

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 numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-38b54ffd07654d4e985484f1b6e74643
Source noteuspto-grants-2014_01