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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375163Generated: November 3, 2026

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

https://huagongshe.com/reaction/2375163

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), and the reaction mixture was stirred at room temperature for 30 minutes. The reaction was then cooled to 5° C. and 2-chloromethyl-pyridine-3-carboxylic acid methyl ester of Step A was added slowly, the temperature 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 numberUS07465722B2
Source datasetuspto-grants-2008_12
ORD IDord-bc4ae229e31d45b2a594b097bbdb262d
Source noteuspto-grants-2008_12