HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-Methylhomoveratrylamine → 3,4-Dichloro-N-[4-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]butyl]-N-(1-methylethyl)benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-Methylhomoveratrylamine | HCID 77039 | — |
| Edukt | N-isopropyl-N-(4-oxobutyl)-3,4-dichlorobenzenesulfonamide | HCID 13770967 | — |
| Katalysator | Adams' catalyst | HCID 345198 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3,4-Dichloro-N-[4-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]butyl]-N-(1-methylethyl)benzenesulfonamide | HCID 13770968 | — |
Reaktionsschritte
The aldehyde prepared in the preceding paragraph (8.90 g, 0.027 m) and N-methyl-homoveratrylamine (5.29 g, 0.027 m) in absolute ethanol (100 ml) containing PtO2 (0.6 g) was shaken under hydrogen (7 hours) and the reaction filtered and stripped to provide the crude product (13.32 g) as a dark greenish gum. This material was chromatographed, after removal of a small amount of insoluble solid, on dry column silica gel (500 g) with 30% methanol/70% ethyl acetate to provide the title compound (7.26 g) as a clear white gum.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04618711 |
| Quelldatensatz | uspto-grants-1986_10 |
| ORD ID | ord-fe203a9032f446659f56f459b8ba90a1 |
| Quellennotiz | uspto-grants-1986_10 |