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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708584Generated: November 2, 2026

Sodium borohydride → HCID 70145591, compound

https://huagongshe.com/reaction/1708584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Acetoxy-5-androstene-17-oneHCID 11759318—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 70145591HCID 70145591—

Reaction Steps

To a solution of 100 mg. (0.303 mmol) of 3-acetoxy-androst-5-en-17-one, 1, 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. Proton NMR confirmed the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359071
Source datasetuspto-grants-1994_10
ORD IDord-3de1789497774da389169364e910595d
Source noteuspto-grants-1994_10