HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl- → Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl- | HCID 3060390 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl- | HCID 3060392 | 50.3% |
Reaction Steps
A solution of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine (4.4 g, 14.1 mM) in methanol (250 ml) was hydrogenated at 1 atmosphere and ambient temperature over 5% palladium on charcoal (500 mg) until the theoretical uptake of hydrogen had occurred (about 2 hours). The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Recrystallisation of the residue from IPA gave the title compound (2 g) m.p. 174°-5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04325953 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-087ae6c0a6d144b4b3419ed8322470da |
| Source note | uspto-grants-1982_04 |