HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl 2-cyano-3-(p-fluorophenyl)glutarate → Ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl 2-cyano-3-(p-fluorophenyl)glutarate | HCID 10935698 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate | HCID 11161405 | 46.3% |
Reaction Steps
5 g of diethyl 2-cyano-3-(p-fluorophenyl)glutarate obtained in Examples 1 to 3 was added to a mixture of 1.4 g of a commercially available developed Raney nickel and 120 mL of ethanol, and the reaction mixture was allowed to react at 27° C. for 6 hours under a hydrogen pressure of 2.5 atm (gauge pressure) of hydrogen. The reaction mixture was filtered through Celite, and the filtrate was concentrated. The resulting oily substance was recrystallized to obtain 2 g of ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate as a crystalline white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197960B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-88cdf4c127224585b6c28cef0be7f266 |
| Source note | uspto-grants-2001_03 |