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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464668Generated: October 25, 2026

Trifluoromethanesulfonic acid → HCID 18930391, compound

https://huagongshe.com/reaction/1464668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
ReactantMethyl 5-(4-chlorophenyl)-1H-pyrrole-2-carboxylateHCID 18930419—
SolventDichloromethaneHCID 6344—
ProductHCID 18930391HCID 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 mi) 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 numberUS05306827
Source datasetuspto-grants-1994_04
ORD IDord-00a9a22d06cf41818bdf98bfba73226a
Source noteuspto-grants-1994_04