HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 19603257, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Chloro-8-hydroxy-2-methylquinoline | HCID 12219722 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | HCID 19603257 | HCID 19603257 | — |
Reaction Steps
The mixture of 4-chloro-8-hydroxy-2-methylquinoline 600 mg), piperidine (6.13 ml) and tetrabutylammonium iodide (10 mg) was refluxed for 18 hours. The cooled reaction mixture was concentrated in vacuo and to the residue was added chloroform and aqueous sodium bicarbonate solution. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from n-hexane to give 8-hydroxy-2-methyl-4-piperidinoquinoline (712 mg) as pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994368 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-09d1cada42f340588466542cc80a9720 |
| Source note | uspto-grants-1999_11 |