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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274299Generated: October 31, 2026

Acetic Anhydride → (15alpha)-15-(Acetyloxy)androst-4-ene-3,17-dione

https://huagongshe.com/reaction/274299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant15alpha-Hydroxyandrost-4-ene-3,17-dioneHCID 11652383—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product(15alpha)-15-(Acetyloxy)androst-4-ene-3,17-dioneHCID 57023990—

Reaction Steps

168 g of 15α-hydroxy-4-androstene-3,17-dione in 250 ml of pyridine and 125 ml of acetic anhydride are heated on a steam bath. After 90 minutes, the reaction mixture is stirred into ice/water. The thus-precipitated product is suctioned off, taken up in methylene chloride, washed with water, and dried over sodium sulfate. After recrystallization from ethyl acetate, 120 g of 15α-acetoxy-4-androstene-3,17-dione is obtained, mp 145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389624
Source datasetuspto-grants-1995_02
ORD IDord-f75258ca317d4ca98f55479aa6368edc
Source noteuspto-grants-1995_02