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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532632Generated: October 31, 2026

Sodium borohydride → HCID 14320346, compound

https://huagongshe.com/reaction/1532632

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 ½ 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. Proton NMR confirmed the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204273B1
Source datasetuspto-grants-2001_03
ORD IDord-e130a9e34b814f16aa1eee7a6e5403c9
Source noteuspto-grants-2001_03