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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 반응물 | 3beta-Tribenzylsilyloxy-7beta-hydroxy-15beta,16beta-methylene-5-androsten-17-one | HCID 70466968 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3beta-Tribenzylsilyloxy-5,6beta-epoxy-7beta-hydroxy-15beta,16beta-methylene-5beta-androstan-17-one | HCID 88686820 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04614616 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-91d96e7f9f5f4930bc6681db0aea5d9e |
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| 출처 메모 | uspto-grants-1986_09 |
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