돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64716생성일: 2026년 10월 24일

Sodium Stearate → 16beta-Ethyl-17beta-stearoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/ko/reaction/64716

반응식

참여 물질

역할이름HCID투입량
반응물Sodium StearateHCID 2724691—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물16beta-Ethyl-17beta-stearoyloxyacetoxy-4-estren-3-oneHCID 7046745057.1%

반응 단계

To 150 ml of acetone-water (2:1) are added 1.3 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 1.0 g of sodium stearate and the mixture is refluxed for 4 hours and allowed to stand at room temperature (15°-25° C.) overnight. The solvent is then distilled off under reduced pressure and the residue is extracted with 150 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure and the residue is dissolved in 100 ml of ethanol. To the solution is added 0.3 g of activated carbon and the insoluble material is filtered off. The solvent is distilled off to give a colorless viscous oil, which is allowed to stand at room temperature (15°-25° C.) to give 1.1 g of the above-identified compound as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609650
출처 데이터셋uspto-grants-1986_09
ORD IDord-0682f4085c25476da26e2c16fc402b56
출처 메모uspto-grants-1986_09