HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ammonia
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-Acetylpiperidin-2-one | HCID 11815905 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 1-(4-Aminopiperidin-1-yl)ethan-1-one | HCID 4962477 | — |
Reaction Steps
0.88 Ammonia (85 ml) was added to a solution of N-acetylpiperidone (15 g, 106 mmol) in methanol (120 ml), followed by palladium hydroxide (2 g) and the mixture hydrogenated at room temperature and 60 psi for 18 hours. The reaction mixture was filtered through Arbocel®, the filtrate concentrated under reduced pressure and the residue azeotroped with toluene to give a yellow oil. The crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (96:3.5:0.5 to 84:14:2) to afford the title compound as a clear oil, 9.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060836B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-3aeb0bdf566a4404b998247c8e514b62 |
| Source note | uspto-grants-2006_06 |