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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1070431Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1070431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrole-2-carboxaldehydeHCID 13854—
EduktSodium hydrideHCID 24758—
EduktMethyl 2-(chloromethyl)pyridine-3-carboxylateHCID 19081344—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylateHCID 53438888—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06903091B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-662d44bfb8db4d6eb0b0c73fecd7464d
Quellennotizuspto-grants-2005_06