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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894502Generated: October 26, 2026

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

https://huagongshe.com/reaction/894502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
ReactantHypofluorous acid, trifluoromethyl esterHCID 78989—
ReactantSodium TrifluoroacetateHCID 517019—
Reactant3beta, 17beta-Di(trifluoroacetoxy)-5alpha-androstaneHCID 86734962—
SolventTrichlorofluoromethaneHCID 6389—
Product3beta,17beta-Di(trifluoroacetoxy)-9alpha-fluoro-5alpha-androstaneHCID 8673496139.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284558
Source datasetuspto-grants-1981_08
ORD IDord-d677881fb3ef4d35b175ab87e500a362
Source noteuspto-grants-1981_08