HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054145Generated: October 27, 2026
Pyrrole-2-carboxaldehyde → Methyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylate
https://huagongshe.com/reaction/2054145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-(chloromethyl)pyridine-3-carboxylate | HCID 19081344 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07329653B2 |
|---|
| Source dataset | uspto-grants-2008_02 |
|---|
| ORD ID | ord-695a59d9cea24d05be77a141d7a92a36 |
|---|
| Source note | uspto-grants-2008_02 |
|---|