HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(chloromethyl)-1-(methylsulfonyl)-1h-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Chloromethylbenzimidazole | HCID 78571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(chloromethyl)-1-(methylsulfonyl)-1h-benzimidazole | HCID 265673 | 63.8% |
Reaction Steps
To a solution of 2-(chloromethyl)benzimidazole (80 g, 0.48 mol) and methanesulfonyl chloride (58.3 mL, 0.75 mol) in 0.5 L of methylene chloride, triethylamine (136 mL, 0.97 mol) was added dropwise under nitrogen. The resulting mixture was stirred at room temperature for 6 hours. The mixture was filtered and the filtrate was evaporated. The residue was triturated in methanol and filtered to afford 74.9 g of the title compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908936B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-dbba3128943e4d57ad430e63766d3b56 |
| Source note | uspto-grants-2005_06 |