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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64713생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Octanoic AcidHCID 379—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물16beta-Ethyl-17beta-n-octanoyloxyacetoxy-4-estren-3-oneHCID 70466981—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609650
출처 데이터셋uspto-grants-1986_09
ORD IDord-fc929792369a463e95c40cc536834624
출처 메모uspto-grants-1986_09