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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)acrylonitrile | HCID 67776130 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)propanenitrile | HCID 67775171 | 80.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637536B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-11328ee3dd9d4d91ae9e09eba409cea1 |
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| Source note | uspto-grants-2014_01 |
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