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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375191Generated: October 26, 2026

Trifluoromethanesulfonic acid → Methyl 5-(p-chlorophenyl)-4-[(trifluoromethyl)thio]pyrrole-2-carboxylate

https://huagongshe.com/reaction/375191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
ReactantMethyl 5-(4-chlorophenyl)-1H-pyrrole-2-carboxylateHCID 18930419—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(p-chlorophenyl)-4-[(trifluoromethyl)thio]pyrrole-2-carboxylateHCID 18930391902.7%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Trifluoromethanesulfonic acid (0.27 g, 0.001795 mol) is added to a solution of methyl 5-(p-chlorophenyl)pyrrole-2-carboxylate (4.23 g, 0.01795 mol) in methylene chloride (70 mL) at -30° C. This mixture is treated with trifluoromethylsulfenyl chloride (4.0 g, 0.0293 mol), stirred for 30 minutes at -15° C., warmed to room temperature with stirring for three hours, diluted with methylene chloride, washed with saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain the title product as an off-white solid (5.44 g, mp 133°-137° C.) which is identified by 1HNMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484807
Source datasetuspto-grants-1996_01
ORD IDord-e48c24ae54374763aa48a8a36b0eeb51
Source noteuspto-grants-1996_01