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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494675Generated: October 30, 2026

Androstenedione → HCID 67830240, compound

https://huagongshe.com/reaction/1494675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAndrostenedioneHCID 6128—
ReactantHCID 57090946HCID 57090946—
SolventAcetone CyanohydrinHCID 6406—
ProductHCID 67830240HCID 67830240—

Reaction Steps

4-Androsten-3,17-dione (20 g) is dissolved by gentle warming in acetone cyanohydrin (30 ml). The crystals which form after several minutes are filtered, washed with pentane, and then dissolved in a mixture of pyridine (50 ml) and acetic anhydride (50 ml). After 48 hours the volatiles are removed under reduced pressure. The residue is then dissolved in ether and washed successively with 5% hydrochloric acid and aqueous sodium bicarbonate. The organic solution is dried and concentrated to afford a mixture of C-17 epimers of 17-cyano-17-acetoxyandrost-4-ene-3-one. Chromatography affords 17β-Cyano-17α-acetoxyandrost-4-ene-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026882
Source datasetuspto-grants-1991_06
ORD IDord-20c4a82b8b734aa4a39a2d9bc968f4e6
Source noteuspto-grants-1991_06