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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614998Generated: October 30, 2026

Acetic Anhydride → HCID 15586530, compound

https://huagongshe.com/reaction/614998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14823693HCID 14823693—
ProductHCID 15586530HCID 15586530—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1.5 g of 9-fluoro-11β-hydroxy-17-(methylsulfinyl)androsta-1,4,16-trien -3-one, 70 ml of acetic anhydride and 2 g of fused sodium acetate is heated at 110° C. under nitrogen for 2 hours. The acetic anhydride is partially removed by distillation under vacuum and the resulting slurry is diluted with 1:1 chloroform-water. The organic layer is separated, washed with diluted sodium bicarbonate solution, water, dried over anhydrous sodium sulfate and evaporated in vacuo. The residue is dissolved in 4:1 chloroform-hexane and chromatographed on a 40 g-silica gel column. Elution with 1:4 hexane-chloroform gives 940 mg of slightly impure material. Two crystallizations from acetone-hexane give 350 mg of the title compound, melting point 193°-194° C., with consistent spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146538
Source datasetuspto-grants-1979_03
ORD IDord-1e7b2cce9feb448595080ac1588ab066
Source noteuspto-grants-1979_03