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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Chloro-4-hydroxy-5-methoxybenzaldehyde | HCID 29000 | — |
| Edukt | 4-(1H-benzoimidazol-2-ylmethoxy)-5-chloro-2-fluoro-benzaldehyde | HCID 59803854 | — |
| Produkt | 4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehyde | HCID 59803890 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07872018B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-fc39b84c238541d1868b16b5ef595e9e |
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| Quellennotiz | uspto-grants-2011_01 |
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