HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(1-Benzylpiperidin-3-yliden)-butyronitrile → 4-(1-Benzylpiperidin-3-ylidene)-butylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(1-Benzylpiperidin-3-yliden)-butyronitrile | HCID 53987194 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(1-Benzylpiperidin-3-ylidene)-butylamine | HCID 70159544 | — |
Reaction Steps
8.0 g (33.3 mmol) 4-(1-benzylpiperidin-3-ylidene)-butyronitrile are dissolved in 80 ml ethanol and added to a spatula tip of Raney-Nickel. The mixture is stirred under hydrogen atmosphere until consumption of the theoretical amount of hydrogen to be taken up (ca. 5 days). The mixture is filtered from the catalyst and the solvent is removed under vacuum. The residue is chromatographically purified Voice over silica gel with CHCl3/CH3OH/NH4OH (90/10/1). After drawing off the solvent, a colorless oil remains which is further processed without additional purification. Yield. 3.9 g (47%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451816B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-7c05bd4657534792bcff8dc8480c28f0 |
| Source note | uspto-grants-2002_09 |