HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 18357113, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-(5-cyanopyridin-2-yloxy)piperidine-1-carboxylate | HCID 57027834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18357113 | HCID 18357113 | 31.4% |
Reaction Steps
To 1-(t-butyloxycarbonyl),4-(5-cyano,2-pyridinyloxy)piperidine (1.6 g) in dichloromethane (20 mL) was added trifluoroacetic acid (1.2 mL) and the reaction stirred at room temperature for 1 hour. The reaction was quenched by evaporation of trifluoroacetic acid dissolving the residue in water, basifying with sodium hydrogen carbonate and extracting the dichloromethane. The organic layer was then washed with water, brine, dried (MgSO4) and evaporated to yield 4-(5-cyano,2-pyridyloxy)piperidine as a white crystalline solid (337 mg), MS: m/z 279 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313127B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-8d9c80c641f047d8be3eeae9f4cc71c9 |
| Source note | uspto-grants-2001_11 |