HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 11372470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-(3-Acetylphenyl)-1-phenyl-5-trifluoromethylbenzimidazole | HCID 11428935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11372470 | HCID 11372470 | — |
Reaction Steps
To a suspension of 7-(3-acetylphenyl)-1-phenyl-5-trifluoromethylbenzimidazole (0.95 g, 2.5 mmol) in ethanol (10 ml) was added sodium borohydride (0.1 g, 2.6 mmol) and the resultant mixture was stirred at 60° C. for 20 min. The cooled reaction mixture was concentrated under reduced pressure and the concentrate was partitioned between ethyl acetate and water. The organic layer was dried over magnesium sulphate and concentrated to a small volume (1-2 ml) under reduced pressure. The title product precipitated upon addition of ligroin to the concentrate (0.65 g, 68%) m/z, 383.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700638B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-239daf1ea2b144a9995990f6769d72fe |
| Source note | uspto-grants-2010_04 |