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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64723생성일: 2026년 10월 24일

N,N-Dimethylaniline → 16beta-Ethyl-17beta-cyclopentylacetoxyacetoxy-4-estren-3-one

https://huagongshe.com/ko/reaction/64723

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Ethyl AcetateHCID 8857—
반응물Cyclopentylacetyl chlorideHCID 3485182—
반응물16beta-Ethyl-17beta-glycoloyloxy-4-estren-3-oneHCID 70466441—
용매DichloromethaneHCID 6344—
생성물16beta-Ethyl-17beta-cyclopentylacetoxyacetoxy-4-estren-3-oneHCID 70467431—

반응 단계

In 10 ml of dichloromethane are dissolved 0.5 g of 16β-ethyl-17β-glycoloyloxy-4-estren-3-one and 0.2 ml of N,N-dimethylaniline and, with stirring, 0.3 ml of cyclopentylacetyl chloride is added. The mixture is stirred at room temperature (15°-25° C.) overnight and 150 ml of ethyl acetate is added. The mixture is washed with 10% H3PO4, water, 10% aqueous NaHCO3, water and saturated aqueous sodium chloride solution in that order and dried over anhydrous magnesium sulfate. The solvent is then distilled off and the residue is subjected to column chromatography. Following passage of 80 ml of diisopropyl ether-n-hexane (1:10), elution is carried out with 80 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.1 g of the above-identified compound as a colorless viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609650
출처 데이터셋uspto-grants-1986_09
ORD IDord-a7eafb5a9e0f40e9a62afd5c8aa56723
출처 메모uspto-grants-1986_09