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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703248Generated: November 1, 2026

p-Toluenesulfenyl chloride → Methyl 5-(4-methylphenylthio)pyrrole-3-carboxylate

https://huagongshe.com/reaction/1703248

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfenyl chlorideHCID 11019146—
Reactantmethyl 1H-pyrrole-3-carboxylateHCID 12361759—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(4-methylphenylthio)pyrrole-3-carboxylateHCID 1289702828.5%

Reaction Steps

Methyl pyrrole-3-carboxylate (2.5 g., 20 mmoles) was dissolved in 50 ml. of methylene chloride. To the stirred solution there was added dropwise p-toluenesulfenyl chloride (2.92 g., 20 mmoles), with the temperature maintained below 30° C. by occasional cooling with an ice-water bath. The reaction was stirred for 60 minutes at room temperature. The reaction mixture was concentrated in vacuo to an oil. The residue was taken up in a mixture of isopropyl alcohol and hexane, a small amount of gum removed by filtration and the filtrate reevaporated in vacuo to an oil (5.0 g.). The latter was chromatographed on 150 g. of silica gel, with 100 ml. fractions of the benzene eluant collected. Fractions 10 to 19 were combined to yield the desired product (1.41 g.) contaminated with an impurity showing a mass spectral peak at 281. The latter was removed by recrystallization from methylene chloride/hexane to yield purified methyl 5-(4-methylphenylthio)pyrrole-3-carboxylate (1.14 g., m.p. 118°-121° C., m/e 247).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351843
Source datasetuspto-grants-1982_09
ORD IDord-4d6e421197ce42b49cf602ddb980af5e
Source noteuspto-grants-1982_09