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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034932Generated: November 1, 2026

Acetic Anhydride → 3beta-Hydroxyandrostane-11,17-dione acetate

https://huagongshe.com/reaction/1034932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3beta-Hydroxy-androstane-11,17-dioneHCID 21968764—
SolventPyridineHCID 1049—
Product3beta-Hydroxyandrostane-11,17-dione acetateHCID 8662566966.4%

Reaction Steps

Acetic anhydride (16.6 g, 162.8 mmol) is added to a solution of Compound 1.14 (33.0 g, 108.55 mmol) in pyridine (150 mL) at 0° C. under an inert atmosphere. The resulting reaction mixture is stirred overnight at ambient temperature. Upon completion of the reaction, as evidenced by TLC, pyridine and remaining acetic anhydride are removed under vacuum. The crude residue is diluted with ethyl acetate (500 mL) and washed with water (3×150 mL), saturated brine solution (100 mL) and dried over MgSO4 (75 g). The solvent is evaporated under vacuum and the crude material is purified by column chromatography [59(W)×800(L) mm, 60-120 Mesh silica, 150 g], eluting with ethyl acetate/hexane (1:10) [25 mL fractions, 10 mL/min elution, monitored by TLC with p-anisaldehyde charring; Rf for Compound 1.15=0.38 and Rf for Compound 1.14=0.1 in EtOAc/Hexane (3:7)] to afford Compound 1.15 (19.0 g, 66.4% yield) as a colorless solid. Table 4 describes the measured properties of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546367B2
Source datasetuspto-grants-2013_10
ORD IDord-2603d9a594b049d6a9401f3003235476
Source noteuspto-grants-2013_10