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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342951Generated: November 1, 2026

Sodium borohydride → HCID 54050151, compound

https://huagongshe.com/reaction/342951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54345374HCID 54345374—
SolventEthanolHCID 702—
ProductHCID 54050151HCID 5405015173.9%

Reaction Steps

A mixture of 4-[2-nitro-4-trifluoromethylbenzoyl]-5-cyclopropylisoxazole (8.00 g) and sodium borohydride (0.53 g) in ethanol (250 ml) was stirred at room temperature for 2 hours. The solution was evaporated almost to dryness and the resultant solution was diluted with ethyl acetate. The solution was washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness. The residue was purified by chromatography on silica eluted with a mixture of ether and petroleum ether to give 4-[hydroxy-(2-nitro-4-trifluoromethylphenyl)methyl]-5-cyclopropylisoxazole (compound 294, 5.95 g) as an off white solid: m.p. 76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859283
Source datasetuspto-grants-1999_01
ORD IDord-8232f34c3ae64ed19992bd2ecc1e99a6
Source noteuspto-grants-1999_01