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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64705생성일: 2026년 10월 24일

N,N-Dimethylaniline → 16beta-Ethyl-17beta-(2-bromopropionyloxy)-4-estren-3-one

https://huagongshe.com/ko/reaction/64705

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Ethyl AcetateHCID 8857—
반응물Propanoyl bromide, 2-bromo-HCID 79047—
반응물OxendoloneHCID 443947—
용매DichloromethaneHCID 6344—
생성물16beta-Ethyl-17beta-(2-bromopropionyloxy)-4-estren-3-oneHCID 86740979—

반응 단계

In 70 ml of dichloromethane are dissolved 3.0 g of 16β-ethyl-17β-hydroxy-4-estren-3-one and 1.6 ml of N,N-dimethylaniline and, with stirring, 1.2 ml of α-bromopropionyl bromide is added to the above solution. The mixture is stirred at room temperature (15°-25° C.) for 30 hours followed by addition of 300 ml of ethyl acetate. The mixture is washed with 10% sulfuric acid and saturated aqueous sodium chloride solution in that order 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 300 ml of diisopropyl ether-n-hexane (1:1), elution is carried out with 600 ml of diisopropyl ether. The eluate is evaporated under reduced pressure to remove the solvent, giving 2.7 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-f6b3b723c1f442e696db14178b654489
출처 메모uspto-grants-1986_09