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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184481Generated: October 26, 2026

Pyrrole-2-carboxaldehyde → Methyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylate

https://huagongshe.com/reaction/2184481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-(chloromethyl)pyridine-3-carboxylateHCID 19081344—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylateHCID 53438888—

Reaction Steps

To a suspension of sodium hydride (5.8 g, 0.12 mol) in dry N,N-dimethyl formamide (25 mL) was added slowly under nitrogen a solution of pyrrole 2-carboxaldehyde (10.5 g, 0.11 mol) in N,N-dimethylformamide (10 mL). The reaction mixture was stirred at room temperature for 30 minutes, then cooled to 5° C. and 2-chloromethyl-pyridine-3-carboxylic acid methyl ester of Step A added slowly while the temperature was being maintained at or below 20° C. After the addition was complete the reaction was stirred at room temperature for 30 minutes. The mixture was evaporated to dryness, and the residue was dissolved in ethyl acetate (250 mL). This solution was washed with water and dried over anhydrous magnesium sulfate. The solvent was then removed in vacuo leaving a dark crystalline solid (23.4 g), which was purified by chromatography on silica gel eluting with a gradient of ethyl acetate/petroleum ether to provide the title compound as a tan crystalline solid (13.75 g), m.p. 91-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900200B2
Source datasetuspto-grants-2005_05
ORD IDord-b557bb844b9349e186e37a9aebf5900c
Source noteuspto-grants-2005_05