HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894046Generated: October 29, 2026
Water → Methyl 5-(2-methylbenzoyl)pyrrole-3-carboxylate
https://huagongshe.com/reaction/894046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Methylbenzoyl chloride | HCID 70276 | — |
| Reactant | methyl 1H-pyrrole-3-carboxylate | HCID 12361759 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 5-(2-methylbenzoyl)pyrrole-3-carboxylate | HCID 12897056 | — |
Reaction Steps
Under nitrogen at room temperature, methyl pyrrole-3-carboxylate (2.5 g., 20 mmoles) was combined with 75 ml. of methylene chloride. o-Toluoyl chloride (3.09 g., 20 mmoles) in 25 ml. of methylene chloride was added, followed by stannic chloride (4.6 ml., 40 mmoles) added at a fast dropwise rate via a needle and syringe. Progress of the reaction was followed by thin layer chromatography (silica gel with ethyl acetate-1/hexane-5/5% acetic acid as eluant). After stirring at room temperature for 2.5 hours, the reaction was cooled with an ice-water bath while 75 ml. of water was added dropwise. After addition was complete, the mixture was stirred for 15 minutes at room temperature, approximately an equal volume of ether was added, the organic layer separated, washed in sequence with water, 1 N sodium hydroxide, water and saturated brine, dried over anhydrous sodium sulfate, filtered and evaporated to yield methyl 5-(2-methylbenzoyl)pyrrole-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282242 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-7a46ed905ec1441cbe7ac4438debce87 |
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| Source note | uspto-grants-1981_08 |
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