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 | — |
Reaction Steps
A mixture of 1-benzyl-4-piperidone (7.2 g, 39.64 mmol), and pyrrolidine (4.23 g, 59.5 mmol) in toluene (50 mL) is refluxed for 4 hr with a Dean-Stark trap to remove water. The mixture is cooled to rt and removal of solvent in vacuo provides the title compound as a light orange oil, which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795262B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-be3916b3255e4de69e525fa9f4d8317c |
| Source note | uspto-grants-2010_09 |