HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 382513Erstellt: 24. Oktober 2026
Sodium hydride → (E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazole
https://huagongshe.com/de/reaction/382513
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Chloro-3-(trifluoromethyl)pyridine | HCID 589833 | — |
| Edukt | 2-[(E)-2-phenylethenyl]-1H-benzimidazole | HCID 5708003 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | (E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazole | HCID 22736647 | 5% |
Reaktionsschritte
To a stirred solution of (E)-2-styryl-1H-benzimidazole (0.49 g, 2.2 mmol) in dimethylacetamide (20 ml) at 0° C. under a nitrogen atmosphere was added sodium hydride (0.11 g, 2.8 mmol). After stirring at 0° C. for 20 min. and then at room temperature for 30 min., a solution of 2-chloro-3-trifluoromethylpyridine (0.60 g, 3.3 mmol) in dimethylacetamide (5 ml) was added. The resulting mixture was heated to reflux for about 3 h 20 min. After cooling, copper bronze (0.45 g, 7.1 mg-atom) was added and heating was continued for 9 h 20 min. The reaction mixture was filtered through a pad of celite and the filtrate was diluted with dichloromethane (200 ml), washed consecutively with water (3×200 ml) and brine (100 ml), dried (magnesium sulfate) and concentrated to dryness. Purification by column chromatography (silica gel, 150 g; n-hexane/ethyl acetate (2/1)) followed by recrystallization from a mixture of isopropyl ether and n-hexane yielded 37 mg (5%) of the titled compound as white solids.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06310079B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-b84f5879348b4393850fb728e75dac59 |
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| Quellennotiz | uspto-grants-2001_10 |
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