HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate → 4-Oxo-piperidine-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate | HCID 102624 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Oxo-piperidine-3-carboxylic acid ethyl ester | HCID 107316 | 88.4% |
Reaction Steps
To a solution of ethyl 1-benzyl-4-oxopiperidine-3-carboxylate (360.0 g, 1.21 mol) in EtOH (6.7 L) was added wet Pd/C (55.0 g) under N2 that then was replaced by H2. The reaction mixture was stirred at rt for 4 h, filtered and concentrated to give a crude product. The crude product was slurried with EtOH (200 mL) for 2 h and then filtered. The filtered cake was washed with MTBE and the combined organic phases were concentrated to give the title compound (222.0 g, 1.07 mol, 88.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09255096B1 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-e33d861d862540c89f7e6b56f0a739a1 |
| Source note | uspto-grants-2016_02 |