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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370801Generated: October 31, 2026

1-(Chlorosulfanyl)-2,3,4,5,6-pentafluorobenzene → HCID 12832379, compound

https://huagongshe.com/reaction/370801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chlorosulfanyl)-2,3,4,5,6-pentafluorobenzeneHCID 119749—
ReactantHCID 12832387HCID 12832387—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 12832379HCID 12832379—

Reaction Steps

Under agitation and using argon as the protective gas, 15 ml of about 1.6N n-butyllithium in hexane, diluted with 30 ml of toluene, is added dropwise at -5° to 0° to a solution of 8.83 g of 4,5-bis(4-methoxyphenyl)-1-(tetrahydropyran-2-yl)imidazole in a mixture of 75 ml of absolute tetrahydrofuran and 75 ml of toluene. After 20 minutes, the pentafluorophenylsulfenyl chloride solution is added dropwise to the reaction mixture, maintaining the temperature between -5° and 0° by cooling. After 2 hours' stirring at room temperature, the solution is diluted with 200 ml of ethyl acetate, washed with sodium bicarbonate solution; the organic solution is dried over sodium sulfate and concentrated to dryness under vacuum. The residue is purified by chromatography on aluminum oxide, neutral, activity stage II, with hexane/ethyl acetate. Recrystallization from ethyl acetate/hexane yields 8.86 g of 4,5-bis(4-methoxyphenyl)-1-(tetrahydropyran-2-yl)-2-(pentafluorophenylthio)imidazole, mp 156°-158°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528298
Source datasetuspto-grants-1985_07
ORD IDord-2159ec690e684f85aab055a31a11dbf4
Source noteuspto-grants-1985_07