HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-Benzylideneaniline → N-Methylbenzylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-Benzylideneaniline | HCID 10858 | — |
| Edukt | Ethenamine, 2-phenyl- | HCID 155076 | — |
| Katalysator | Cobalt | HCID 104730 | — |
| Produkt | N-Methylbenzylamine | HCID 7669 | — |
| Produkt | Benzylaniline | HCID 66028 | — |
Reaktionsschritte
Imines were hydrogenated using in situ-generated complex 2. Hydrogenation of N-benzylidene benzylamine proceeded under 4 atm H2 at 60° C. to afford dibenzylamine in 84% isolated yield using 2 mol % of complex 2 (Table 2, entry 13). N-Benzylidenemethylamine and N-benzylideneaniline were also hydrogenated by the cobalt catalyst, affording N-benzyl methyl amine and N-benzylaniline in good yields (Table 2, entries 14 and 15). Previous examples of cobalt-catalyzed imine hydrogenation are scarce.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09434666B2 |
| Quelldatensatz | uspto-grants-2016_09 |
| ORD ID | ord-4a4db7e6614b4d4ab660ea8ce57cdbad |
| Quellennotiz | uspto-grants-2016_09 |