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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010703Generated: November 4, 2026

Sodium borohydride → HCID 59674980, compound

https://huagongshe.com/reaction/1010703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67313333HCID 67313333—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 59674980HCID 5967498075.4%

Reaction Steps

To a solution of 56 mg (0.13 mmol) of 5-(3-chlorophenyl)-3-(2-fluoro-5-trifluoromethyl-phenyl)-4-[(3-pyridyl)carbonyl]isoxazole in 2 mL of ethanol was added 24 mg (0.63 mmol) of sodium borohydride. After 2 hrs at room temperature, the reaction mixture was diluted with ethyl acetate. The solution was washed with saturated sodium chloride and was dried over magnesium sulfate. The drying agent was filtered off, and solvent was removed by rotoevaporation. The residue was purified by prepTLC to give 44 mg (0.098 mmol) of 5-(3-chlorophenyl)-3-(2-fluoro-5-trifluoromethylphenyl)-4-[(3-pyridyl)hydroxymethyl]isoxazole. 1H NMR (CDCl3): δ 6.01 (s, 1), 7.01 (m, 1), 7.83 (m, 1), 8.27 (m, 1), and 8.35 ppm (br s, 1). MS m/z: 449.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977341B2
Source datasetuspto-grants-2011_07
ORD IDord-0b98207ad34f483b90e82c4747227acb
Source noteuspto-grants-2011_07