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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2184449Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2184449

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-dimethylformamide (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 as such in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06900200B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-41d5697da93844aaa9123f1992552625
Quellennotizuspto-grants-2005_05