HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824970Generated: October 30, 2026
Sodium borohydride → 3-(5-Trifluoromethylbenzofur-7-yl)-2-butanol
https://huagongshe.com/reaction/1824970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(5-Trifluoromethylbenzofur-7-yl)-2-butanone | HCID 22144922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(5-Trifluoromethylbenzofur-7-yl)-2-butanol | HCID 22144864 | 45.4% |
Reaction Steps
A solution of 0.09 gm (0.35 mMol) 3-(5-trifluoromethylbenzofur-7-yl)-2-butanone in ethanol was cooled to 0° C. To this solution was added 0.013 gm (0.35 mMol) sodium borohydride and the resulting mixture stirred for 30 minutes. The reaction mixture was then allowed to warm to room temperature and was concentrated under reduced pressure. The residue was taken up in ethyl acetate and washed sequentially with 0.1 N hydrochloric acid, water, and saturated aqueous sodium chloride. The remaining organic phase was concentrated under reduced pressure and the residue subjected to silica gel chromatography, eluting with 30% ethyl acetate in hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 0.041 gm (45%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045545B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-5d44e87683e240ccb6b7652de52247e5 |
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| Source note | uspto-grants-2006_05 |
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