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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705840Generated: October 30, 2026

Sodium borohydride → 3-(4-(4-Fluorophenoxy)phenyl)propanenitrile

https://huagongshe.com/reaction/705840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-(4-Fluorophenoxy)phenyl)acrylonitrileHCID 67775820—
SolventEthanolHCID 702—
Product3-(4-(4-Fluorophenoxy)phenyl)propanenitrileHCID 6777581279%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-(4-(4-fluorophenoxyl)phenyl)acrylonitrile (5 g, 20.90 mmol) in ethanol (80 mL) was added NaBH4 (5.44 g, 144 mmol). The mixture was heated at 70° C. overnight. After cooling to room temperature, the reaction mixture was quenched with water (50 mL), and ethanol was removed under reduced pressure. The residue was partitioned between EA (100 mL) and water (50 mL). The organic phase was washed with saturated NaHCO3 solution (80 mL), brine (50 mL), dried over sodium sulfate, concentrated, and purified via flash chromatography to afford the title compound (4.7 g, 16.48 mmol, 79% yield) as a white solid. LCMS: rt=1.55 min, [M+H+]=242

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-0f1c2cd9d4984ff399041dca9556c11a
Source noteuspto-grants-2015_11