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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474602Generated: October 30, 2026

Sodium borohydride → 3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)propanenitrile

https://huagongshe.com/reaction/474602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)acrylonitrileHCID 67776130—
SolventEthanolHCID 702—
Product3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)propanenitrileHCID 6777517180.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-(4-(3-(trifluoromethyl)phenoxy)phenyl)acrylonitrile (5 g, 17.29 mmol) in Ethanol (80 mL) was added NaBH4 (4.5 g, 119 mmol). The reaction mixture was stirred 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 (4.3 g, 13.89 mmol, 80% yield) as colorless oil. LCMS: rt=1.64 min, no MS signal

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-11328ee3dd9d4d91ae9e09eba409cea1
Source noteuspto-grants-2014_01