돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64706생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/64706

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Ethyl AcetateHCID 8857—
반응물2-Bromo-2-methylpropionyl bromideHCID 88685—
반응물OxendoloneHCID 443947—
용매DichloromethaneHCID 6344—
생성물16beta-Ethyl-17beta-(2-bromo-2-methylpropionyloxy)4-estren-3-oneHCID 70467305—

반응 단계

In 30 ml of dichloromethane are dissolved 3.2 g of 16β-ethyl-17β-hydroxy-4-estren-3-one and 1.2 ml of dimethylaniline and, with stirring at room temperature (15°-25° C.), 1.0 ml of 2-bromo-2-methylpropionyl bromide is added to the above solution. The mixture is stirred at room temperature (15°-25° C.) for 16 hours, followed by addition of 300 ml of ethyl acetate. The mixture is washed with 10% phosphoric acid, water, 5% aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride 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 400 ml of diisopropyl ether-n-hexane (1:1), elution is carried out with 800 ml of the same solvent system. The eluate is evaporated under reduced pressure to remove the solvent, giving 2.6 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-21598c1f3df748a9a17a46da1a1ea233
출처 메모uspto-grants-1986_09