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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975208Generated: October 25, 2026

1,2-Dichloroethane → 2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole

https://huagongshe.com/reaction/1975208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
ReactantHCID 10448068HCID 10448068—
SolventDichloromethaneHCID 6344—
Product2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrroleHCID 1893040672%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 2-(p-chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrrole (2.47 g, 0.0080 mol), trifluoromethylsulfenyl chloride (2.18 g, 0.016 mol), trifluoromethanesulfonic acid (0.12 g, 0.0008 mol) and 1,2-dichloroethane (15 mL) is placed in a pressure tube, heated at 70° C. for five days, diluted with methylene chloride, washed with saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain an amber syrup. Flash chromatography of the syrup using silica gel and a 1:5 ethyl acetate/hexanes solution gives the title product as an off-white solid (2.36 g, mp 118°-122° C.) which is identified by 1HNMR and 13CNMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284863
Source datasetuspto-grants-1994_02
ORD IDord-54142b4b8e154dbb8c92c1b70a9d17f9
Source noteuspto-grants-1994_02