HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(1H-Benzimidazol-1-yl)-N-benzylpropan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 3-(1H-1,3-benzodiazol-1-yl)propan-1-amine | HCID 3920849 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1H-Benzimidazol-1-yl)-N-benzylpropan-1-amine | HCID 20469054 | — |
Reaction Steps
0.5 Gram of 10% palladium on charcoal was prehydrogenated in 100 ml. of absolute ethanol until the uptake of hydrogen stopped. Then, a solution of 10 grams of 1H-benzimidazole-1-propanamine and 6.7 grams of benzaldehyde in 50 ml. of absolute ethanol was added and the mixture was stirred at atmospheric pressure and room temperature under hydrogen until the calculated amount of hydrogen was taken up. The catalyst was then removed by filtration and the solvent was evaporated to leave N-benzyl-1H-benzimidazole-1-propanamine as a colorless oil. This material was sufficiently pure for further reaction but, if desired, a pure sample could be obtained by column chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04363808 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-5ab23850e9a44aa79a3e87306aef8c55 |
| Source note | uspto-grants-1982_12 |