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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65417생성일: 2026년 10월 24일

tert-Butyl hydroperoxide → 3beta-Tribenzylsilyloxy-5,6beta-epoxy-7beta-hydroxy-15beta,16beta-methylene-5beta-androstan-17-one

https://huagongshe.com/ko/reaction/65417

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl hydroperoxideHCID 6410—
반응물3beta-Tribenzylsilyloxy-7beta-hydroxy-15beta,16beta-methylene-5-androsten-17-oneHCID 70466968—
용매TolueneHCID 1140—
생성물3beta-Tribenzylsilyloxy-5,6beta-epoxy-7beta-hydroxy-15beta,16beta-methylene-5beta-androstan-17-oneHCID 88686820—

반응 조건

온도80 °C

반응 단계

24 g of 3β-tribenzylsilyloxy-7β-hydroxy-15β,16β-methylene-5-androsten-17-one is dissolved in 50 ml of toluene, combined with 500 mg of vanadium(IV) oxide acetylacetonate, and heated to 80° C. A solution of 75 ml tert.-butyl hydroperoxide (10 ml 80% tert.-butyl hydroperoxide in 100 ml of toluene) is added dropwise to the reaction mixture, and the latter is allowed to stand for 1.5 hours at this temperature. After cooling, the mixture is washed with water and saturated sodium chloride solution, dried, and evaporated under vacuum, thus obtaining 24.5 g of 3β-tribenzylsilyloxy-5,6β-epoxy-7β-hydroxy-15β,16β-methylene-5β-androstan-17-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614616
출처 데이터셋uspto-grants-1986_09
ORD IDord-91d96e7f9f5f4930bc6681db0aea5d9e
출처 메모uspto-grants-1986_09