HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
9,10-Anthracenedione, 1-bromo-4-(methylamino)- → 1-Methylamino-4-(p-trifluoromethoxy-anilino)-anthraquinone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 9,10-Anthracenedione, 1-bromo-4-(methylamino)- | HCID 31418 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | 4-(Trifluoromethoxy)aniline | HCID 600848 | — |
| Katalysator | Cupric acetate | HCID 8895 | — |
| Produkt | 1-Methylamino-4-(p-trifluoromethoxy-anilino)-anthraquinone | HCID 21425074 | — |
Reaktionsbedingungen
| Temperatur | 132 °C |
|---|
Reaktionsschritte
12.64 parts of 1-methylamino-4bromo-anthraquinone, 9.9 parts of para-trifluoromethoxyaniline, 6 parts of potassium acetate and 2 parts of copper acetate are introduced into 43 parts of 4-methyl-2-pertanol and the mixture is heated at 132° C. for 8 hours. The mixture is then cooled to 60° C., filtered, washed with water, then the precipitate is taken up in dilute caustic soda, filtered, washed and dried. 9.6 parts of 1-methylamino-4-(p-trifluoromethoxy-anilino)-anthraquinone are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04035397 |
| Quelldatensatz | uspto-grants-1977_07 |
| ORD ID | ord-ac64c7d594e14581bcbb8eb574d9b28c |
| Quellennotiz | uspto-grants-1977_07 |