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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2-MercaptobenzimidazoleHCID 707035—
Edukt2-Chloro-1,3-thiazole-5-carbaldehydeHCID 1479765—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehydeHCID 5982574670,7%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163768B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-8774921c530b4d5aabd29eb07c113f19
Quellennotizuspto-grants-2012_04