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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616642Generated: October 25, 2026

Ethanol → Androsta-5,16-dien-3 beta-ol

https://huagongshe.com/reaction/616642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodiumHCID 5360545—
Reactant(3S,8R,9S,10R,13S,14S)-17-iodo-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta(a)phenanthren-3-olHCID 11069352—
SolventWaterHCID 962—
ProductAndrosta-5,16-dien-3 beta-olHCID 150900—

Reaction Steps

125 g. of sodium metal were added in small portions to a stirred solution of 21 g. of 3β-hydroxy-17-iodo androsta-5,16-diene in 1.05 l. of anhydrous ethanol. During the addition the mixture was kept at reflux temperature. After all of the sodium was dissolved the reaction mixture was cooled and water was added. The ethanol was removed by distillation under reduced pressure and the resulting aqueous suspension was extracted with methyl isobutyl ketone. The extract was washed until neutral and concentrated to dryness in vacuo. The crystalline residue was recrystallized from methanol-water and 13 g. of 3β-hydroxy-androsta-5,16-diene were obtained. Two crystallizations from acetone yielded the pure compound melting at 137°-138° C. mol. peak in mass spectrum (m/e): 272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075233
Source datasetuspto-grants-1978_02
ORD IDord-0614c3ad5e564a9aa4f6399ba41cc9a6
Source noteuspto-grants-1978_02