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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64708Generated: October 27, 2026

16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one → 16beta-Ethyl-17beta-propionyloxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
ReactantPotassium propionateHCID 23663619—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product16beta-Ethyl-17beta-propionyloxyacetoxy-4-estren-3-oneHCID 1342041435.4%

Reaction Steps

In a mixture of 50 ml of acetone and 12 ml of water are dissolved 2.5 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 0.7 g of potassium propionate. The solution is stirred at room temperature (17°-25° C.) for 3 days and concentrated under reduced pressure. The residue is extracted with 200 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 1000 ml isopropyl ether-n-hexane (2:3), elution is carried out with 2000 ml of the same solvent system. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.87 g of the above-identified compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-a8f40c9d274a414588b143f5af3ffad3
Source noteuspto-grants-1986_09