Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595960Generated: October 30, 2026

Acetic Anhydride → HCID 57133820, compound

https://huagongshe.com/reaction/1595960

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 an oil. [α]D22=+20.00 (c=0.51% in chloroform)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288051B1
Source datasetuspto-grants-2001_09
ORD IDord-bda974ac20004003b3e147871ab7ac03
Source noteuspto-grants-2001_09