HuagongsheHuagongshe Chemistry Print Report · For research reference only
18-Crown-6 → 1-(2-Chlorobenzyl)-2-methylbenzimidazole-6-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | 1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl- | HCID 22620342 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(2-Chlorobenzyl)-2-methylbenzimidazole-6-acetonitrile | HCID 18680981 | 43% |
Reaction Steps
Potassium cyanate (0.450 g) and 0.450 g of 18-crown-6 were added to a solution of 1.20 g of 1-(2-chlorobenzyl)-6-chloromethyl-2-methylbenzimidazole in 10 ml of dimethylsulfoxide, and the mixture was stirred at room temperature for 18 hours. The reaction mixture was extracted with the addition of chloroform, water and a small amount of aqueous ammonia. The organic layer was concentrated, and the residue was purified through silica-gel column chromatography (eluent: a mixture of chloroform and methanol at a ratio of 20:1) to give 0.500 g of 1-(2-chlorobenzyl)-2-methylbenzimidazole-6-acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-4ec5c6e3e3b14b689ae0ae8c0e55b205 |
| Source note | uspto-grants-2002_03 |