HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylate → Ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylate | HCID 104608 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate | HCID 104609 | — |
Reaction Steps
A solution of 59 g of 1-carbethoxy-4-(2-nitro-4-chloroanilino)-piperidine in 270 ml of tetrahydrofuran and 96 ml of absolute ethanol was hydrogenated under normal pressure and at room temperature, using 15 g of Raney nickel as a catalyst. When the uptake of hydrogen had ended, the mixture was filtered and the filtrate was evaporated. Melting point: 150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470989 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-cd3198adf58c421e8c4c8a6348df186c |
| Source note | uspto-grants-1984_09 |