HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-[(2'-Carbomethoxybiphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(2'-Carbomethoxybiphenyl-4-yl)methyl-2-butyl-4-chloroimidazole-5-carboxaldehyde | HCID 15698069 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[(2'-Carbomethoxybiphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole | HCID 11004192 | — |
Reaction Steps
A solution of 4.8 g of 2-butyl-4-chloro-5-formyl-1-[(2'-methoxycarbonyl-1,1'-biphenyl-4-yl)methyl]-1H-imidazole in 100 ml of absolute ethanol is added with a solution of 0.44 g of NaBH4 in 10 ml of ethanol. The mixture is stirred at room temperature for 1 hour then is acidified with glacial CH3COOH to pH 4. The resulting solution is evaporated to dryness under reduced pressure and the residue is taken up into ether. The in soluble part is filtered, the ether solution is evaporated to dryness and the residue is stripped more times with toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538987 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-4c6f921d6cb74cdebb6522867fbdd0ae |
| Source note | uspto-grants-1996_07 |