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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253455Erstellt: 26. Oktober 2026

Dimethylformamide → 4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehyde

https://huagongshe.com/reaction/253455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt2-Chloro-4-hydroxy-5-methoxybenzaldehydeHCID 29000—
Edukt4-(1H-benzoimidazol-2-ylmethoxy)-5-chloro-2-fluoro-benzaldehydeHCID 59803854—
Produkt4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehydeHCID 59803890—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2-Chloro-4-hydroxy-5-methoxy-benzaldehyde (136, 2.30 g, 0.0123 mol) was dissolved in N,N-dimethylformamide (89.5 mL, 1.16 mol) and sodium hydride (60% dispersion in mineral oil, 541 mg, 0.0135 mol) was added. After 20 minutes, 2-chloromethyl-1H-benzoimidazole (106, 2.05 g, 0.0123 mol) was added to the reaction. The reaction was stirred at 80° C. overnight. The reaction was concentrated in vacuo to an oil. Ethyl acetate was added and washed with saturated sodium bicarbonate and brine. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 30-70% ethyl acetate in hexane over 30 minutes to provide a white solid (137, 1.79 g, 46%). MS (ESI) [M+H+]+=317.1, 319.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872018B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-fc39b84c238541d1868b16b5ef595e9e
Quellennotizuspto-grants-2011_01