HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | 1-Carbethoxyazepan-4-one | HCID 12666086 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate | HCID 15037322 | 100% |
Reaction Steps
A mixture of 46 parts of ethyl hexahydro-4-oxo-1H-azepine-1-carboxylate, 26 parts of benzenemethanamine, 2 parts of a solution of thiophene in methanol 4% and 400 parts of methanol was hydrogenated at normal pressure and at room temperature with 4 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, yielding 69.1 parts (100%) of ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate as a residue (interm. 27).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04988689 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-5b4de34054044b898b5cfe2297e92abb |
| Source note | uspto-grants-1991_01 |