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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64713Generated: October 23, 2026

Octanoic Acid → 16beta-Ethyl-17beta-n-octanoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/en/reaction/64713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanoic AcidHCID 379—
Reactant16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product16beta-Ethyl-17beta-n-octanoyloxyacetoxy-4-estren-3-oneHCID 70466981—

Reaction Steps

In 60 ml of acetone is dissolved 1.0 ml of n-octanoic acid, and 3.0 ml of 2N-NaOH, 15 ml of water and 1.8 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one are serially added to the above solution. The mixture is refluxed for 4 hours. The solvent is distilled off under reduced pressure and the residue is extracted with 150 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 50 ml of diisopropyl ether, elution is carried out with 300 ml of the same solvent. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.7 g of the above-identified compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-fc929792369a463e95c40cc536834624
Source noteuspto-grants-1986_09