Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Anilinopiperidine | HCID 89982 | — |
Reaction Steps
In a three neck round bottom flask equipped with mechanical stirrer and water condenser, 15.36 gm (o.10 moles) of 4-piperidone hydrochloride monohydrate and 9.3 gm (0.10 moles) of aniline were added. To this mixture, 6.5 gm (0.10 moles) of zinc and 0.6 gm (0.10 moles) of 90% acetic acid were added. The reaction mixture was stirred at room temperature for 24 hrs and at 50 to 70° C. for 24 hrs. Water was then added to the reaction mixture and filtered. Crushed ice was added to the filtrate and was neutralized with excess of aqueous sodium hydroxide solution. The crude 4-anilinopiperidine was obtained by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399677B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-28205c74abd14c16b9e1b4c8ce420d5e |
|---|
| Source note | uspto-grants-2013_03 |
|---|