HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-(N-Boc-amino)piperidine → 4-(N-Boc-amino)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-(N-Boc-amino)piperidine | HCID 4438618 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Palladium | HCID 23938 | — |
| Product | 4-(N-Boc-amino)piperidine | HCID 723833 | 95.2% |
Reaction Steps
1-Benzyl-4-t-butyloxycarbonylaminopiperidine (Method D, 5.4 g, 18.6 mmol) was dissolved in absolute ethanol (100 ml) and hydrogenated over 10% Pd/C for 24 hours at ambient temperature. The catalyst was removed by filtration and the filtrates evaporated to give the title compound (3.54 g, 17.7 mmol) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878712B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-e4e21712af8b4dd390e165f5b87dea96 |
| Source note | uspto-grants-2005_04 |