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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524972Generated: October 29, 2026

O-Toluidine → 3-Methyl-N-o-tolyl-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/524972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantOxalyl chlorideHCID 65578—
Reactant3-methyl-1H-pyrrole-2-carboxylic acidHCID 7140352—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Methyl-N-o-tolyl-1H-pyrrole-2-carboxamideHCID 7092227987%

Reaction Steps

2.0 g (15.98 mmol) of 3-methyl-1H-pyrrole-2-carboxylic acid were dissolved in 50 mL of dichloromethane. 5.60 mL (63.9 mmol) of oxalyl chloride were added, followed by 5 drops of DMF. The reaction mixture was stirred at room temperature for 2 hours and then the solvents were evaporated. The black oil residue was dissolved in 50 mL of dichloromethane and 6.85 g (63.9 mmol) of o-toluidine were added dropwise. The reaction was stirred at room temperature for 1 hour and then the solvent was evaporated. The crude product was purified by flash chromatography (dichloromethane to dichloromethane/methanol 95:5) and then triturated in diisopropylether to give 2.97 g (87% yield) of the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340547B2
Source datasetuspto-grants-2016_05
ORD IDord-f236cc4087e84bb6a79ccd2afd49b8c4
Source noteuspto-grants-2016_05