HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(5-bromopyridin-2-yl)-1H-imidazole-4-carbaldehyde | HCID 86614005 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol | HCID 68511931 | 70.6% |
Reaction Steps
To a suspension of 1-(5-bromopyridin-2-yl)-1H-imidazole-4-carbaldehyde (730 mg, 2.90 mmol) in MeOH (10 mL) at room temperature was added NaBH4 (134 mg, 3.53 mmol). The mixture was stirred for 30 min, during which time the suspension became clear. The solvent was removed in vacuo. The residue was partitioned between H2O and EtOAc. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol as a solid (520 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696352B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-7e810aad404940188a7f1a0bc6802032 |
| Source note | uspto-grants-2010_04 |