HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-(4-Nitrophenyl)-4-piperidinol → 1-(4-Aminophenyl)piperidin-4-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-(4-Nitrophenyl)-4-piperidinol | HCID 613768 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | HCID 178418390 | HCID 178418390 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(4-Aminophenyl)piperidin-4-ol | HCID 16792107 | — |
Reaktionsschritte
The 4-hydroxy-N-(4-nitrophenyl)piperidine (11.1 g, 50 mmol) obtained in Example 1(1) was dissolved in methanol (100 ml) and tetrahydrofuran (50 ml), and 10% palladium-carbon (8.0 g) was added thereto, followed by stirring at room temperature in an atmosphere of hydrogen gas for 7 hours. After the insoluble material was filtered with Celite, the filtrate was concentrated under reduced pressure, diethyl ether was added to the obtained residue, and the precipitate was collected by filtration, thereby obtaining 4-hydroxy-N-(4-aminophenyl)piperidine (9.25 g, 94%) as a reddish-purple solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08865714B2 |
| Quelldatensatz | uspto-grants-2014_10 |
| ORD ID | ord-fbcaf3d7bfc54d948e4b438198483c19 |
| Quellennotiz | uspto-grants-2014_10 |