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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371809생성일: 2026년 10월 24일

Diethyl Ether → 17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3beta-ol

https://huagongshe.com/ko/reaction/371809

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물19-HydroxytestosteroneHCID 150968—
반응물Aluminium lithium hydrideHCID 21226445—
반응물17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3-oneHCID 86735678—
용매TetrahydrofuranHCID 8028—
생성물17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3beta-olHCID 86735677—

반응 단계

The compound 17β,19-dihydroxyandrost-4-en-3-one is similarly etherified to form the 17β-OR4, 19-OR1, derivatives of androst-4-en-3-one. Reduction as previously described yields the corresponding 3-hydroxy analogues. For example, 17β,19-dihydroxyandrost-4-en-3-one is converted to 17β,19-di-triphenylsiloxyandrost-4-en-3-one and 17β,19-di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3-one as previously described. These compounds are then reduced using lithium aluminum hydride in an ether or tetrahydrofuran solution to produce 17β,19-di-triphenylsiloxyandrost-4-en-3β-ol and 17β,19-di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3β-ol, respectively.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04087524
출처 데이터셋uspto-grants-1978_05
ORD IDord-c843252dc8e045bd9c6a786e7333510e
출처 메모uspto-grants-1978_05