HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[[(3-Methyl-4-nitro 2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)-3-methyl-4-nitropyridine | HCID 16095904 | — |
| Reactant | HCID 178506086 | HCID 178506086 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[[(3-Methyl-4-nitro 2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazole | HCID 23036499 | — |
Reaction Steps
A solution of 9.4 g of 2-(chloromethyl)-3-methyl-4-nitropyridine and 10 g of 5-(trifluoromethyl)-2-benzimidazolethiol in 260 ml of abs. acetone was treated with 3 g of finely ground potassium carbonate and stirred at room temperature under argon for 18 hours. 180 ml of acetone were distilled off in a vacuum, whereupon the remaining portion of the reaction mixture was poured on to ice. The crystallized-out product was filtered off and dried at 35° in a drying oven By recrystallization from ethyl acetate/n-hexane there was obtained 2-[[(3-methyl-4-nitro 2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazole of melting point 192°-193°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04950677 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-723fb6bb14e74e0091b3883e992ce6aa |
| Source note | uspto-grants-1990_08 |