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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 328208생성일: 2026년 10월 26일

Hydrogen Peroxide → (17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-ol

https://huagongshe.com/reaction/328208

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Sodium borohydrideHCID 4311764—
반응물16alpha,17alpha-Epoxy-3-methoxy-18-methyl-1,3,5(10)-estratrieneHCID 86734624—
반응물HCID 178528034HCID 178528034—
용매EthanolHCID 702—
생성물(17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-olHCID 86734623—

반응 조건

온도0 °C

반응 단계

3.7 g. of diphenyldiselenide is dissolved in 200 ml. of absolute ethanol and combined at room temperature with 1.0 g. of sodium borohydride. After the yellow solution has lost its color, 5.0 g. of 16α,17α-epoxy-3-methoxy-18 -methyl-1,3,5(10)-estratriene is added thereto and the mixture is heated under reflux for 30 hours. The solution is then cooled to 0° C. Dropwise, 11ml. of 30% H2O2 is added to the reaction solution and the latter is then gradually heated to 50° C. After 2 hours, the solution is introduced into ice water. The precipitate is vacuum-filtered, washed with water, and taken up in methylene chloride. After chromatography on silica gel with 6-8% acetone/hexane, 1.9 g. of 3-methoxy-18-methyl-1,3,5(10),15-estratetraen-17α-ol is obtained as an oily product. [α]D 20 = -108°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04016269
출처 데이터셋uspto-grants-1977_04
ORD IDord-47443581362643fe9d5aadc35279fb3a
출처 메모uspto-grants-1977_04