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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694641Generated: October 30, 2026

Sodium borohydride → HCID 57800077, compound

https://huagongshe.com/reaction/1694641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-[3-(trifluoromethyl)phenyl]-1,2-oxazole-3-carboxylateHCID 53439058—
SolventEthanolHCID 702—
ProductHCID 57800077HCID 57800077—

Reaction Steps

To a stirred solution of ethyl 5-[3-(trifluoromethyl)phenyl]isoxazole-3-carboxylate (2 g, 7 mmol) in ethanol (70 mL) in an ice bath was added sodium borohydride (1.06 g, 28 mmol) portionwise. The resulting mixture was stirred at room temperature for 1.5 hours, which was then quenched with saturated ammonium chloride aqueous solution. Solvent was removed from the mixture under reduced pressure, and the residue was dissolved in ethyl acetate and washed with water. The organic layer was then dried over sodium sulfate, and solvent removed under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:Hexanes=2:3) to afford {5-[3-(trifluoromethyl)phenyl]isoxazol-3-yl}methane-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158810B2
Source datasetuspto-grants-2012_04
ORD IDord-87273f60050641de958f51eba6d1818a
Source noteuspto-grants-2012_04