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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980916Generated: November 1, 2026

Water → Methyl 5-(2-methylbenzoyl)pyrrole-3-carboxylate

https://huagongshe.com/reaction/1980916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant2-Methylbenzoyl chlorideHCID 70276—
Reactantmethyl 1H-pyrrole-3-carboxylateHCID 12361759—
SolventDiethyl EtherHCID 3283—
ProductMethyl 5-(2-methylbenzoyl)pyrrole-3-carboxylateHCID 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, 1N 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511575
Source datasetuspto-grants-1985_04
ORD IDord-8cda3cb91c144964beeccc6aed82b057
Source noteuspto-grants-1985_04