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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260041Generated: October 31, 2026

Sodium borohydride → HCID 14320346, compound

https://huagongshe.com/reaction/260041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Acetoxy-5-androstene-17-oneHCID 11759318—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 14320346HCID 14320346—

Reaction Steps

To a solution of 100 mg (0.303 mmol) of 3-acetoxy-androst-5-en-17-one in 3 ml EtOH at -10° C., was added 22.9 mg (0.606 mmol) of sodium borohydride with stirring. After the reaction mixture was stirred for one and 1/2 hours, the mixture was diluted with 10 ml water, the ethanol solvent removed under vacuum, and the residue extracted with ethyl acetate. The organic layer was washed with aqueous Na2CO3, brine, dried over sodium sulfate and concentrated to leave a residue of crude title compound. The proton NMR was in accord with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05525608
Source datasetuspto-grants-1996_06
ORD IDord-0528e7b4a89c49b2b50d441846664538
Source noteuspto-grants-1996_06