HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → Methyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Methyl 3-methyl-4-oxopiperidine-1-carboxylate | HCID 3015586 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylate | HCID 19785254 | — |
Reaction Steps
A mixture of 26 parts of methyl 3-methyl-4-oxo-1-piperidinecarboxylate, 16.5 parts of benzenemethanamine, 2 parts of a solution of thiophene in ethanol 4% and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated to dry, yielding 40.2 parts of methyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylate as a residue (interm. 26).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041448 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-60772a1c2ec74ad4add8f86192d94ffc |
| Source note | uspto-grants-1991_08 |