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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830082Generated: October 26, 2026

Pyrrole-2-carboxaldehyde → 1-[(4,5-Dimethoxy-2-nitrophenyl)methyl]-1H-pyrrole-2-carboxaldehyde

https://huagongshe.com/reaction/1830082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-2-nitro-4,5-dimethoxybenzeneHCID 3016812—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-[(4,5-Dimethoxy-2-nitrophenyl)methyl]-1H-pyrrole-2-carboxaldehydeHCID 31082794.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (0.724 g, 60% suspension in oil) in N,N-dimethyl formamide (50 mL) was added pyrrole 2-carboxaldehyde (1.7 g, 18.1 mmol) and the reaction mixture was stirred for 30 minutes. It was then cooled to 0° C. and 4,5-dimethoxy-2-nitrobenzyl bromide (5.0 g, 1 equiv) was added dropwise over 20 minutes. After the addition, the reaction mixture was stirred at room temperature for 3 hours. It was then diluted with ethyl acetate (450 mL), washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness. The crude product was triturated with water, filtered and washed with water. This material was dried over anhydrous potassium carbonate in vacuo to provide the title compound as a yellow crystalline solid (4.97 g), m.p. 109–112° C., which was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064120B2
Source datasetuspto-grants-2006_06
ORD IDord-de69308d13b94d25955dcf6a5286b132
Source noteuspto-grants-2006_06