HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705799Generated: October 30, 2026
Water → 3-(3-Bromo-4-fluorophenyl)propanenitrile
https://huagongshe.com/reaction/705799
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (E)-3-(3-Bromo-4-fluorophenyl)acrylonitrile | HCID 61702072 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(3-Bromo-4-fluorophenyl)propanenitrile | HCID 53434301 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174968B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7bae86022e174a06989fd226a8c83e4e |
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| Source note | uspto-grants-2015_11 |
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