HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-benzylpiperidine-4-carboxylate → HCID 18399772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-benzylpiperidine-4-carboxylate | HCID 90423 | — |
| Reactant | Thiopheneethanamine | HCID 116521 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18399772 | HCID 18399772 | — |
Reaction Steps
22.15 g of ethyl 1-benzyl-4-piperidinecarboxylate and 1 equivalent of the product obtained in Step B are added to a solution of 4.12 g of sodium in 103 ml of anhydrous ethanol. After 12 hours reaction at reflux, the reaction mixture is evaporated. The residue is taken up in dichloromethane and washed with water, and then the organic phase is dried, filtered and evaporated, enabling an oil to be obtained which crystallises in diisopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399616B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-1765bd76b6124b36bcea42c2e51873d1 |
| Source note | uspto-grants-2002_06 |