HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703256Generated: October 26, 2026
methyl 1H-pyrrole-3-carboxylate → HCID 12897036, compound
https://huagongshe.com/reaction/1703256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | methyl 1H-pyrrole-3-carboxylate | HCID 12361759 | — |
| Reactant | 2,5-Dichlorobenzenesulfenyl chloride | HCID 12878541 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12897036 | HCID 12897036 | — |
Reaction Steps
Under a nitrogen atmosphere, methyl pyrrole-3-carboxylate (2.5 g., 20 mmoles) was dissolved in 50 ml. of methylene chloride and cooled with stirring in an ice-water bath. 2,5-Dichlorobenzenesulfenyl chloride (4.24 g., 20 mmoles) was added dropwise. The bath was removed and the reaction stirred for 1 hour at room temperature, at which time thin layer chromatography (silica gel with ethyl acetate-1/hexane-5/5% acetic acid as eluant) indicated that virtually all of the starting pyrrole ester had been consumed. An equal volume of ether was added, the mixture filtered and the filtrate evaporated in vacuo to a partially crystalline gum (5.2 g.). The latter was recrystallized from methylene chloride/hexane to yield purified methyl 5-(2,5-dichlorophenylthio)pyrrole-3-carboxylate (2.68 g., m.p. 162°-165° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04351843 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-50dfb80244ea4216bb26013fcc156982 |
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| Source note | uspto-grants-1982_09 |
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