HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 1-Benzofuran-2-yl-2-[5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-benzoimidazol-1-yl]-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-One | HCID 2735451 | — |
| Reactant | 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole | HCID 11651910 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzofuran-2-yl-2-[5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-benzoimidazol-1-yl]-ethanone | HCID 59682300 | — |
Reaction Steps
To 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole (460.5 mg) in DMF (5 mL) was added sodium hydride (103 mg of 60% in oil dispersion). The resulting mixture was stirred at room temperature for 5 min. To the dark green solution was added 1-(1-benzofuran-2-yl)-2-bromoethan-1-one (633 mg) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was quenched with water, extracted with EtOAc, and dried over Na2SO4. The crude product was purified by silica gel chromatography (10%-40% EtOAc/hexanes) to yield the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879895B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-359a5c5aab9a492c8929c0da2df3af27 |
| Source note | uspto-grants-2011_02 |