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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894502생성일: 2026년 10월 24일

Nitrobenzene → 3beta,17beta-Di(trifluoroacetoxy)-9alpha-fluoro-5alpha-androstane

https://huagongshe.com/ko/reaction/894502

반응식

참여 물질

역할이름HCID투입량
반응물NitrobenzeneHCID 7416—
반응물Hypofluorous acid, trifluoromethyl esterHCID 78989—
반응물Sodium TrifluoroacetateHCID 517019—
반응물3beta, 17beta-Di(trifluoroacetoxy)-5alpha-androstaneHCID 86734962—
용매TrichlorofluoromethaneHCID 6389—
생성물3beta,17beta-Di(trifluoroacetoxy)-9alpha-fluoro-5alpha-androstaneHCID 8673496139.4%

반응 단계

A well-stirred solution of 3β, 17β-di(trifluoroacetoxy)-5α-androstane (2.5 g, 5.15 mmole, prepared by treatment of 5α-androstane-3β,17β-diol with trifluoroacetic anhydride in pyridine), nitrobenzene (800 mg, 6.5 mmole) and sodium trifluoroacetate (10 g, 73.5 mmole) in fluorotrichloromethane (45 ml) was treated with trifluoromethyl hypofluorite (8.5 mmole) at -20° for 2.5 hours, air being admitted to the reaction vessel during this time. Thereafter the solution was purged with nitrogen and the solvent was removed in vacuo. The residue was dissolved in chloroform and the resulting solution was washed with aqueous sodium bicarbonate and water and was then dried, whereafter the product was chromatographed on silica gel (125 g). Elution with chloroform:hexane (3:7) gave unreacted starting material (308 mg), while subsequent elution with chloroform:hexane (7:13) gave 3β,17β-di(trifluoroacetoxy)-9α-fluoro-5α-androstane (1.02 g), which crystallised from hexane as prisms (917 mg) m.p. 140°-142°; [α] D24 -22° (c 1.47, CHCl3). (Found C,55.10; H,5.78; F,26.35%;m/e 502. C33H29O4F7 requires C,54.97; H,5.82; F,26.47%; M+ 502).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04284558
출처 데이터셋uspto-grants-1981_08
ORD IDord-d677881fb3ef4d35b175ab87e500a362
출처 메모uspto-grants-1981_08