HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,3-Propanediamine → N-(1-Benzylpiperidin-4-yl)propane-1,3-diamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,3-Propanediamine | HCID 428 | — |
| Edukt | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-(1-Benzylpiperidin-4-yl)propane-1,3-diamine | HCID 3017248 | — |
Reaktionsschritte
The starting material is prepared as follows: To the ice cooled stirred solution of 62.5 ml of 1,3-diaminopropane in 100 ml of ethanol, 30 g of 1-benzyl-4-piperidone are added dropwise. The mixture is hydrogenated over 2 g of pre-reduced platinum oxide at 50° and 2.7 atm. for 9 hours. After theoretical hydrogen-uptake the catalyst is filtered off, the filtrate evaporated, the residue distilled and the fraction boiling at 145°-160°/0.2 mmHg collected, to yield the 4-(3-aminopropylamino)-1-benzylpiperidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04147786 |
| Quelldatensatz | uspto-grants-1979_04 |
| ORD ID | ord-c893534eda664bd0b93af5aadf21ad9e |
| Quellennotiz | uspto-grants-1979_04 |