HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trifluoroacetic acid → 2,3-Bis(4-fluorophenyl)quinoxaline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | O-Phenylenediamine | HCID 7243 | — |
| Edukt | 4,4'-Difluorobenzil | HCID 123072 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 2,3-Bis(4-fluorophenyl)quinoxaline | HCID 2260050 | — |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
For example, in synthetic route `A2` of FIG. 2, 4,4'-difluorobenzil, 1,2-phenylenediamine and chloroform are charged together in a reaction vessel and stirred. A catalytic amount of trifluoroacetic acid is added slowly and the reaction mixture heated to about 50° C. with continued stirring. After about 16 h, the mixture is cooled to provide 2,3-bis(4-fluorophenyl)quinoxaline after removal of the chloroform. Recrystallization results 2,3-bis(4-fluorophenyl)quinoxaline having a melting point of 127-1290° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06124421 |
| Quelldatensatz | uspto-grants-2000_09 |
| ORD ID | ord-64a4ef4dedde49bfa63dd084a1b36a6c |
| Quellennotiz | uspto-grants-2000_09 |