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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371060Generated: October 26, 2026

Trifluoroacetic acid → HCID 70401069, compound

https://huagongshe.com/reaction/371060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 12917712HCID 12917712—
SolventDichloromethaneHCID 6344—
SolventChloroform hexaneHCID 21585165—
ProductHCID 70401069HCID 7040106985.9%

Reaction Steps

To a homogeneous solution of 600 mg (1.66 mmole) of 17-(ethylthio)-9-fluoro-11β-hydroxyandrosta-1,4,16-trien-3-one in a mixture of dry dichloromethane (60 ml) and trifluoroacetic acid (207 mg) was added triethylsilane (230 mg) and the mixture was stirred at room temperature under a nitrogen atmosphere for 2.5 hours. Since the tlc of an aliquot showed incomplete reaction, more trifluoroacetic acid (207 mg) and triethylsilane (230 mg) were added. After 1.5 hours the starting material had disappeared by tlc. The resulting solution was diluted with dichloromethane, washed with saturated sodium bicarbonate solution and water, dried (anhydrous sodium sulfate) and evaporated in vacuo to give a solid. This was redissolved in 1:4 hexane chloroform and chromatographed on a 30 g silica gel column. Elution with 1:4 hexane-chloroform, chloroform and 5:95 ethyl acetate-chloroform gave 520 mg of a tlc-homogeneous title compound. Crystallization from acetone-hexane gave 410 mg of an analytical specimen, melting point 223°-225° C., with consistent spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529548
Source datasetuspto-grants-1985_07
ORD IDord-47aa9269b1f14dc58a4ad14220c8a794
Source noteuspto-grants-1985_07