돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64727생성일: 2026년 10월 25일

Dimethylformamide → 16beta-Ethyl-17beta-n-heptanoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64727

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Heptanoic AcidHCID 8094—
반응물Sodium HydroxideHCID 14798—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물16beta-Ethyl-17beta-n-heptanoyloxyacetoxy-4-estren-3-oneHCID 7046764664%

반응 단계

In 30 ml of acetone is dissolved 2.6 g of n-heptanoic acid, and 10 ml of 2N-NaOH, 4.2 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one, 30 ml of DMF and 10 ml of water are serially added to the above solution. The mixture is refluxed for 5 hours. After cooling, 400 ml of ethyl acetate is added and the mixture is 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 400 ml of diisopropyl ether-n-hexane (2:3), elution is carried out with 1000 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 3.0 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-51711f58cf9043d294756a7ccce7d9b7
출처 메모uspto-grants-1986_09