HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696639Erstellt: 24. Oktober 2026
Sodium hydride → 2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehyde
https://huagongshe.com/de/reaction/1696639
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Mercaptobenzimidazole | HCID 707035 | — |
| Edukt | 2-Chloro-1,3-thiazole-5-carbaldehyde | HCID 1479765 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehyde | HCID 59825746 | 70,7% |
Reaktionsschritte
1,3-Dihydro-benzimidazole-2-thione (1.0 g, 6.66 mmol) is suspended into 50 mL of tetrahydrofuran under argon. Then, 479 mg (9.99 mmol) of sodium hydride is added. The reaction mixture is stirred at room temperature until gas evolution has ceased. 2-Chloro-1,3-thiazole-5-carbaldehyde (983 mg, 6.66 mmol) is then added and the reaction mixture is stirred at room temperature for 2 h, upon which it is filtered. The solid is washed with tetrahydrofuran and dried under reduced pressure. The residue is diluted with water and extracted twice with ethyl acetate and once with dichloromethane. The organic extracts are combined, dried on magnesium sulfate, filtered and concentrated under reduced pressure. 1.23 g of 2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehyde is obtained as a pale yellow powder. mp: 188° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08163768B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-8774921c530b4d5aabd29eb07c113f19 |
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| Quellennotiz | uspto-grants-2012_04 |
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