Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidineacetonitrile, α-phenyl-, hydrochloride (1:1) | HCID 22252850 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22499375 | HCID 22499375 | 72.2% |
Reaction Steps
A mixture of α-phenyl-4-piperidineacetonitrile hydrochloride (0.05 mole), 1-fluoro-4-nitrobenzene (0.06 mole) and potassium carbonate (0.15 mole) in DMF (200 ml) was stirred at 50° C. for four hours. Water and DIPE were added. The mixture was cooled. The precipitate was filtered off, washed with water and DIPE and dried, yielding 11.6 g of (±)-1-(4-nitrophenyl)-α-phenyl-4-piperidine-acetonitrile (intermediate 12, melting point 118° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07169796B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-4d17202151214714ae8bb565a2cb6c2b |
|---|
| Source note | uspto-grants-2007_01 |
|---|
