HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 3-(1-Benzylpiperidin-4-yl)propan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(1-Benzylpiperidin-4-yl)propanenitrile | HCID 19959256 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1-Benzylpiperidin-4-yl)propan-1-amine | HCID 19959205 | 78.6% |
Reaction Steps
A mixture of 3-(1-benzylpiperidin-4-yl)propanenitrile (0.5 g), Raney nickel (0.3 ml) and a conc. ammonia aqueous solution (1 ml) in ethanol (10 ml) was hydrogenated at atmospheric pressure for 6 hours. After Raney nickel was removed by filtration, the filtrate was evaporated in vacuo. The residue was chromatographed on alumina eluting with 2% methanol in chloroform and the fractions containing the object product were collected and evaporated to give 3-(1-benzylpiperidin-4-yl)propylamine (0.4 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622976 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-b684a9927b4f4434827faf834b653fd7 |
| Source note | uspto-grants-1997_04 |