HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 59682295, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole | HCID 11651910 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59682295 | HCID 59682295 | — |
Reaction Steps
To 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole (1 g) in DMF (5 mL) was added sodium hydride (85 mg of 60% in oil dispersion). The resulting mixture was stirred at room temperature for 5 min. To the dark green solution was added ethyl bromoacetate (363 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 (5%-30% EtOAc/hexanes) to yield the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566733B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-605b56681d754246bb14c93bb1eb591f |
| Source note | uspto-grants-2009_07 |