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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64712생성일: 2026년 10월 25일

2-Ethylbutyric acid → 16beta-Ethyl-17beta-(2-ethylbutyryl)oxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64712

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethylbutyric acidHCID 6915—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매AcetoneHCID 180—
용매Sodium HydroxideHCID 14798—
생성물16beta-Ethyl-17beta-(2-ethylbutyryl)oxyacetoxy-4-estren-3-oneHCID 70466967—

반응 단계

In 35 ml of acetone is dissolved 1.0 ml of 2-ethylbutyric acid, and 4.6 ml of 2N-NaOH and then 1.9 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one are added to the above solution. The mixture is refluxed for 3 hours. The acetone is distilled off under reduced pressure and the residue is extracted with two 100 ml portions of ethyl acetate. The organic layers are combined, 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 50 ml of ether, elution is carried out with 300 ml of the same solvent. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.63 g of the above-identified compound as a light-yellow viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609650
출처 데이터셋uspto-grants-1986_09
ORD IDord-685484c6284b41cb99dbeb91de9c8807
출처 메모uspto-grants-1986_09