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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1912709생성일: 2026년 10월 26일

17,17-Bis(ethylendioxy)-5-androsten-7-one → 17,17-Bis(ethylendioxy)androstan-7-one

https://huagongshe.com/reaction/1912709

반응식

참여 물질

역할이름HCID투입량
반응물17,17-Bis(ethylendioxy)-5-androsten-7-oneHCID 67537234—
반응물3beta-Acetoxyandrostane-7,17-dioneHCID 69011313—
용매Ethyl AcetateHCID 8857—
생성물17,17-Bis(ethylendioxy)androstan-7-oneHCID 6895071382%

반응 단계

17,17-Bis(ethylendioxy)androstane-7-one was prepared in 82% yield from 3,3:17,17-bis(ethylendioxy)-5-androsten-7-one by the procedure described above for the preparation of 3β-acetoxyandrostane-7,17-dione (Prepn. 41) using EtOAc instead of EtOH. The crude product was purified by flash chromatography (SiO2, n-hexane/EtOAc 6/4). 1H-NMR (300 MHz, acetone-d6, ppm from TMS: δ 3.96-3.75 (m, 8H), 2.54-1.10 (m, 20H), 1.13 (s, 3H), 0.83 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609644B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-4fd12f5929a54b6da8ab017e2265ee76
출처 메모uspto-grants-2013_12