HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylate → 3-(Boc-amino)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylate | HCID 22258937 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Boc-amino)piperidine | HCID 4233041 | 91% |
Reaction Steps
A mixture of benzyl 3-[(tert-butoxycarbonyl)amino]-1-piperidinecarboxylate (2.25 g, 6.73 mmol) and 10% Pd/C (0.229 g) in EtOH (20 mL) was stirred at room temperature under a hydrogen atmosphere (1 atm) for 14 hrs. The catalyst was removed by filtration through Celite®, and the filtrate was concentrated under reduced pressure to give tert-butyl 3-piperidinylcarbamate as a solid (1.22 g, yield; 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07232909B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-aa853b4b47e6412283b1ae4e6ffba0a9 |
| Source note | uspto-grants-2007_06 |