HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazol-5-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazole-5-carbaldehyde | HCID 15088505 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazol-5-yl)methanol | HCID 15088539 | — |
Reaction Steps
Sodium borohydride (1.1 g, 29 mmole) was added in three portions to a stirred mixture of crude 1-benzyl-4-chloro-5-formyl-2-(4-nitrophenyl)imidazole (54.2 g, 88 mmole) in methanol (250 ml) at room temperature. After two hours, more sodium borohydride (0.51 g, 15 mmol) was added, the mixture was stirred for 30 minutes and the methanol was evaporated. The residue was mixed with water (250 ml) and extracted with methylene chloride (200 ml, 3×50 ml). The combined organic solutions were washed with water (2×50 ml) and dried (NaSO4) overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07182934B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-f8bde9eff2d24d42912c29510dd56676 |
| Source note | uspto-grants-2007_02 |