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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361646Generated: October 31, 2026

Acetic Anhydride → HCID 57133820, compound

https://huagongshe.com/reaction/361646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22941791HCID 22941791—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 57133820HCID 57133820—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 37.7 g of 17β-acetoxy-7α-(5-hydroxypentyl)-estr-4-en-3-one in 160 ml of pyridine is slowly mixed with 80 ml of acetic anhydride and stirred for 16 hours at 25° C. Then, it is diluted with ethyl acetate, and the organic phase, after washing with sodium bicarbonate solution, is dried and concentrated by evaporation. The residue is chromatographed on silica gel, and 26.6 g of 17β-acetoxy-7α-(5-acetoxypentyl)-estr-4-en-3-one is obtained as oil. [α]D22 =+20.0°(c=0.51% in chloroform)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866560
Source datasetuspto-grants-1999_02
ORD IDord-d311cc932c0845a9bbaab8f5ebe2382e
Source noteuspto-grants-1999_02