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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64709Generated: October 28, 2026

Potassium isobutyrate → 16beta-Ethyl-17beta-isobutyryloxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium isobutyrateHCID 23677462—
Reactant16beta-Ethyl-bromoacetoxy-4-estren-3-oneHCID 86740980—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product16beta-Ethyl-17beta-isobutyryloxyacetoxy-4-estren-3-oneHCID 7046730770.8%

Reaction Steps

In a mixture of 50 ml of acetone and 10 ml of water are dissolved 1.5 g of 16β-ethyl-bromoacetoxy-4-estren-3-one and 0.8 g of potassium isobutyrate and the solution is refluxed for 6 hours. The acetone is distilled off under reduced pressure and 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 then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 100 ml of diisopropyl ether, elution is carried out with 300 ml of ethyl ether. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.08 g of the above-identified compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-cdc3ce81002b4065be101e123cbaec2d
Source noteuspto-grants-1986_09