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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64720생성일: 2026년 10월 23일

Water → 16beta-Ethyl-17beta-pivaloyloxyacetoxy-4-estren-3-one

https://huagongshe.com/ko/reaction/64720

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Pivalic acidHCID 6417—
반응물Sodium HydroxideHCID 14798—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매AcetoneHCID 180—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물16beta-Ethyl-17beta-pivaloyloxyacetoxy-4-estren-3-oneHCID 7046739387.3%

반응 단계

In 20 ml of acetone is dissolved 0.61 g of pivalic acid, and 3.0 ml of 2N-NaOH and 10 ml of water are added. And then, 1.2 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 30 ml of DMF are added and the mixture is refluxed for 6 hours. After cooling, 150 ml of ethyl acetate is added and the organic layer is separated. The aqueous layer is is further extracted with 50 ml of ethyl acetate. The organic layers are combined, 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, elution being carried out with 400 ml of diisopropyl ether. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.1 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-e7605e3a96a64f4e8089c5273357f85c
출처 메모uspto-grants-1986_09