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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735642Generated: October 30, 2026

Pyridine → 2,5-Bis[(trifluoromethyl)sulfanyl]-1H-pyrrole

https://huagongshe.com/reaction/1735642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPyrroleHCID 8027—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
CatalystIronHCID 23925—
SolventCarbon DioxideHCID 280—
SolventChloroformHCID 6212—
Product2,5-Bis[(trifluoromethyl)sulfanyl]-1H-pyrroleHCID 12508316—
Product2,4-Bis[(trifluoromethyl)sulfanyl]-1H-pyrroleHCID 12508322—

Reaction Steps

25 g of trifluoromethanesulfenyl chloride was condensed in a pressured bottle in dry ice and 2.34 g of pyrrole in 40 ml of anhydrous chloroform, 12.1 g of pyridine and 0.8 g of iron powder were added. The mixture was then stirred at room temperature for 3 days. It was then filtered to remove insoluble materials. The mixture was washed with water, diluted hydrochloric acid and water again. After evaporation of the solvent, the residue was distilled under vacuum, giving 4.2 g of 2,5-bis(trifluoromethylthio)pyrrole and 3.5 g 2,4-bis(trifluoromethylthio)pyrrole. The total yield was 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538812
Source datasetuspto-grants-1996_07
ORD IDord-97155b9936e34cadbc7e11a8c90454f4
Source noteuspto-grants-1996_07