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 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
Reaction Steps
6 g of Pd/C (10%) are added to a solution of 0.224 mol of tert-butyl 1-benzyl-4-piperidinylcarbamate in 800 ml of anhydrous ethanol. The reaction mixture is placed under a hydrogen pressure of 4 bars, at 50° C., for 48 hours, and then filtered over Celite and concentrated under reduced pressure, enabling the expected product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486171B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-6548b59f40dd43c0a2e75c213bd1e016 |
| Source note | uspto-grants-2002_11 |