HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinecarboxamide → 1-Benzylpiperidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzylpiperidine-4-carboxamide | HCID 783156 | — |
Reaction Steps
A mixture of 20 g (156 mmol) of isonipecotamide, 32.4 g (234 mmol) of potassium carbonate, 2 g (12 mmol) of potassium iodide and 18.6 ml (156 mmol) of benzyl bromide in 400 ml of acetonitrile is heated at reflux for 5 hours. The solvent is evaporated off and the residue is taken up in a dichloromethane/water mixture. After decanting, extracting with dichloromethane, washing the organic phases with brine and drying, removal of the solvent by evaporation yields the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06469011B2 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-96ba61b71a4b45189158cdf50e304565 |
| Source note | uspto-grants-2002_10 |