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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2215129Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2215129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrole-2-carboxaldehydeHCID 13854—
EduktSodium hydrideHCID 24758—
Edukt1-(Bromomethyl)-2-nitro-4,5-dimethoxybenzeneHCID 3016812—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-[(4,5-Dimethoxy-2-nitrophenyl)methyl]-1H-pyrrole-2-carboxaldehydeHCID 31082794,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109193B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-978ca54f673f4a4483a4375c351e2aac
Quellennotizuspto-grants-2006_09