HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → ethyl 4-aminohexahydro-1H-azepine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate | HCID 15037322 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ethyl 4-aminohexahydro-1H-azepine-1-carboxylate | HCID 15037323 | 100% |
Reaction Steps
69.1 Parts of ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate were hydrogenated in the presence of a solution of thiophene in methanol 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 46.9 parts (100%) of ethyl 4-aminohexahydro-1H-azepine-1-carboxylate as a residue (interm. 28).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05151424 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-386185bd730342ad924d9edc84b7a245 |
| Source note | uspto-grants-1992_09 |