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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64716Generated: October 27, 2026

Sodium Stearate → 16beta-Ethyl-17beta-stearoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium StearateHCID 2724691—
Reactant16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product16beta-Ethyl-17beta-stearoyloxyacetoxy-4-estren-3-oneHCID 7046745057.1%

Reaction Steps

To 150 ml of acetone-water (2:1) are added 1.3 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 1.0 g of sodium stearate and the mixture is refluxed for 4 hours and allowed to stand at room temperature (15°-25° C.) overnight. The solvent is then 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 and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure and the residue is dissolved in 100 ml of ethanol. To the solution is added 0.3 g of activated carbon and the insoluble material is filtered off. The solvent is distilled off to give a colorless viscous oil, which is allowed to stand at room temperature (15°-25° C.) to give 1.1 g of the above-identified compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-0682f4085c25476da26e2c16fc402b56
Source noteuspto-grants-1986_09