HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 10971939, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 10928704 | HCID 10928704 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10971939 | HCID 10971939 | 107.7% |
Reaction Steps
A solution of Example 11F (200 mg, 0.431 mmol) in dichloromethane (5 mL) at room temperature was treated with tetrakis(triphenylphosphine)palladium (43 mg, 0.0375 mmol), triphenylphosphine (19.6 mg, 0.075 mmol), piperidine (0.0447 mL, 0.452 mmol), and allowed to stir at room temperature for 30 minutes. The reaction mixture was diluted with 0.5 N HCl, and extracted with dichloromethane. The organic layer was dried (Na2SO4), filtered, concentrated, and purified on silica gel with 10% methanol/CH2Cl2 to provide 197 mg (100%) of the desired compound as an white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288261B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-4eeef9b9f37b42d080cddf34d52f276a |
| Source note | uspto-grants-2001_09 |