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HRID 894502作成日:2026年10月24日

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

https://huagongshe.com/reaction/894502

反応式

関与物質

役割名称HCID仕込み量
反応物NitrobenzeneHCID 7416—
反応物Hypofluorous acid, trifluoromethyl esterHCID 78989—
反応物Sodium TrifluoroacetateHCID 517019—
反応物3beta, 17beta-Di(trifluoroacetoxy)-5alpha-androstaneHCID 86734962—
溶媒TrichlorofluoromethaneHCID 6389—
生成物3beta,17beta-Di(trifluoroacetoxy)-9alpha-fluoro-5alpha-androstaneHCID 8673496139.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284558
出典データセットuspto-grants-1981_08
ORD IDord-d677881fb3ef4d35b175ab87e500a362
出典メモuspto-grants-1981_08