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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259219Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/259219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrobenzeneHCID 7416—
EduktHypofluorous acid, trifluoromethyl esterHCID 78989—
EduktSodium TrifluoroacetateHCID 517019—
Edukt3beta, 17beta-Di(trifluoroacetoxy)-5alpha-androstaneHCID 86734962—
LösungsmittelTrichlorofluoromethaneHCID 6389—
Produkt3beta,17beta-Di(trifluoroacetoxy)-9alpha-fluoro-5alpha-androstaneHCID 8673496139,4%

Reaktionsschritte

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 crystallized from hexane as prisms (917 mg) m.p. 140°-142°; [α] 24D - 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04036864
Quelldatensatzuspto-grants-1977_07
ORD IDord-50793cc9a5b34832bb6f4dd45901331d
Quellennotizuspto-grants-1977_07