HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine → 4-(4,5,6,7-Tetrafluoroindol-3-yl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine | HCID 11395638 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 4-(4,5,6,7-Tetrafluoroindol-3-yl)piperidine | HCID 22615585 | 90% |
Reaction Steps
To a solution of N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine (20.0 g, 49.21 mmol) [prepared as described in Step 1 above] in argon deoxygenated 80% ethanol/tetrahydrofuran (800 ml) was added 10% Pd-C (5 g), and the resulting mixture was stirred under a hydrogen atmosphere (1 atm) for 3 h. The mixture was degassed under argon, filtered through Celite, and concentrated in vacuo. The solid residue was recrystallized from methylene chloride/hexane to afford 4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine (90%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130220 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-5b442c6c4eae48aa969555cbc5ec4a82 |
| Source note | uspto-grants-2000_10 |