HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Ethoxycarbonyl-4-(4'-fluorophenyl)piperidin-6-one | HCID 11140022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate | HCID 11161405 | — |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
3.8 g of the cis/trans mixture of ethyl 4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate obtained in Examples 4 to 6 was added to 100 mL of toluene, and 2.7 mL of a 28% methanol solution of sodium methoxide was added. The reaction mixture was heated at 110° C. for 2.5 hours, then poured into ice water and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to obtain 3.28 g of ethyl trans-4-(p-fluorophenyl)-6-oxo-3-piperidinecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197960B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-70a44cb2713b4d8a8145cb53ec6edc02 |
| Source note | uspto-grants-2001_03 |