HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Methoxy-3-methyl-2-trifluoromethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178488964 | HCID 178488964 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Methoxy-3-methyl-2-trifluoromethylbenzimidazole | HCID 18316636 | 107.3% |
Reaction Steps
To a solution of 4-methoxy-2-trifluoromethylbenzimidazole (1.4 g) in tetrahydrofuran (40 ml) under nitrogen was added sodium hydride (0.32 g; 60% dispersion in oil). The mixture was stirred for 20 minutes at room temperature before methyl iodide (1.35 g) was added. Stirring was continued overnight. The reaction was quenched by the addition of water (10 ml) and the solvent removed in vacuo. Ethyl acetate (50 ml) was added and the organic layer washed with saturated sodium bicarbonate solution (20 ml), water (20 ml) and brine (20 ml). Drying over anhydrous magnesium sulfate followed by the removal of the solvent in vacuo gave the title compound (1.6 g) as an oil which solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353010B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-a444ee7d83814d28be7d6d046cd41d05 |
| Source note | uspto-grants-2002_03 |