HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → N-(4-chlorobenzyl)-3-(2,4-dimethylimidazol-1-yl)propylamine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,4-dimethyl-1H-imidazole-1-propanamine | HCID 13588910 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-chlorobenzyl)-3-(2,4-dimethylimidazol-1-yl)propylamine dihydrochloride | HCID 19429494 | — |
Reaction Steps
In a similar manner to Example 35, a mixture of 4-chlorobenzaldehyde (3.8 g) and 1-(3-aminopropyl)-2,4-dimethylimidazole (4.1 g) in ethanol (70 ml) was stirred and then reduced with sodium borohydride (2.0 g). The hydrochloride salt was triturated with propan-2-ol, filtered and the residue washed with ether, then dried under vacuum at 45° C., to give N-(4-chlorobenzyl)-3-(2,4-dimethylimidazol-1-yl)propylamine dihydrochloride, m.p. 208°-210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05547972 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-fb8b2f78d35149e8bae6f84980b283f4 |
| Source note | uspto-grants-1996_08 |