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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64714Generated: October 26, 2026

Sodium Caprate → 16beta-Ethyl-17beta-n-decanoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CaprateHCID 4457968—
Reactant16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product16beta-Ethyl-17beta-n-decanoyloxyacetoxy-4-estren-3-oneHCID 7046718271.3%

Reaction Steps

To 200 ml of acetone-water (1:1) are added 6.0 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 5.2 g of sodium n-decanoate and the mixture is refluxed for 10 hours. The solvent is distilled off under reduced pressure and the residue is extracted with 300 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 750 ml of diisopropyl ether-n-hexane (1:9), elution is carried out with 1000 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 5.2 g of the above-identified compound as a light-yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-f1c16560236046729a790a84d862926a
Source noteuspto-grants-1986_09