HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 5-Benzoyl-2-(2-pyridylsulfinylmethyl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Benzoyl-2-(2-pyridylthiomethyl)benzimidazole | HCID 13961167 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Benzoyl-2-(2-pyridylsulfinylmethyl)benzimidazole | HCID 13961170 | 66.5% |
Reaction Steps
10.1 g (0.05 mole) of 85% pure m-chloroperoxybenzoic acid are added slowly to a solution, cooled to -15° C., of 17.3 g (0.05 mole) of 5-benzoyl-2-(2-pyridylthiomethyl)benzimidazole in 250 ml of dichloromethane. The mixture is stirred at a temperature below -10° C. for 30 minutes and 100 ml of sodium carbonate solution are added. The organic phase is decanted, washed with sodium carbonate and water and then dried (Na2SO4). When this has been filtered, the solvent is evaporated off and the residue recrystallized in acetone. 12.0 g (66.5%) of 5-benzoyl-2-(2-pyridylsulfinylmethyl)benzimidazole, melting point 142°-145° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791114 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-1e00a93faf7d423bb98d89f236396c8d |
| Source note | uspto-grants-1988_12 |