HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-piperidone → 1-Benzyl-4-(1-pyrrolidinyl)-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Benzyl-4-(1-pyrrolidinyl)-1,2,3,6-tetrahydropyridine | HCID 11746812 | 102% |
Reaction Steps
Pyrrolidine (31.8 mL, 0.38 mol) was added to a solution of 1-benzyl-4-piperidinone (48.0 g, 0.25 mol) in toluene (180 mL) and the mixture refluxed under Dean-Stark conditions for 4.5 hours. The reaction mixture was allowed to cool to room temperature and concentrated under reduced pressure to give the title compound as an orange oil (61.8 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06936619B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-2d7a90af37cf447299565b82df1e22cb |
| Source note | uspto-grants-2005_08 |