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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352870Generated: November 2, 2026

Methanol → Methyl pyrrole-2-carboxylate

https://huagongshe.com/reaction/1352870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyrrole-2-Carboxylic AcidHCID 12473—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantPotassium bisulfateHCID 516920—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductMethyl pyrrole-2-carboxylateHCID 13693079%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 1H-pyrrole-2-carboxylic acid (5.5 g, 49.5 mmol), WSCI.HCl (12.2 g, 63.6 mmol), HOBt (8.4 g, 62.2 mmol), methanol (7.0 g, 218 mmol) and 4-dimethylaminopyridine (3.0 g, 24.5 mmol) in dimethylformamide (60 ml) was stirred for 70 hours at room temperature and for 2 hours at 60° C. To the reaction mixture was added an aqueous 5% potassium hydrogensulfate solution and the mixture was extracted with ethyl acetate/toluene (1/1). The organic layer was washed with an aqueous saturated sodium hydrogencarbonate solution, and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. The solvent was removed and the residue was purified with silica gel chromatography (hexane:ethyl acetate=5:1→3:1) to give the subject compound (4.88 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220773B2
Source datasetuspto-grants-2007_05
ORD IDord-335556ca63294b2fa29f77aaecb7bb12
Source noteuspto-grants-2007_05