Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705844Generated: October 31, 2026

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

https://huagongshe.com/reaction/705844

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 numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-079c2862470441a8a178923bbb4fea6e
Source noteuspto-grants-2015_11