Reaktionsgleichung
[Cl:1][C:2]1[CH:12]=[C:11]([Cl:13])[C:10]([NH:14][C:15]2[C:20]([F:21])=[CH:19][C:18]([F:22])=[CH:17][C:16]=2[Cl:23])=[CH:9][C:3]=1[C:4]([O:6]CC)=[O:5].S(=O)(=O)(O)O>C(O)C>[Cl:1][C:2]1[CH:12]=[C:11]([Cl:13])[C:10]([NH:14][C:15]2[C:20]([F:21])=[CH:19][C:18]([F:22])=[CH:17][C:16]=2[Cl:23])=[CH:9][C:3]=1[C:4]([OH:6])=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
120 mg (0.31 mmol) of ethyl 2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoate were suspended in 6 ml of an ethanol/2 N sodium hydroxide solution mixture (1:1) and heated at 90° C. for 3 hours. After cooling to room temperature, the pH was adjusted to 2 with 2 N sulfuric acid, and the precipitate was filtered off with suction. 98 mg (88%) of the product were obtained.
Aufarbeitung
- temperatureAfter cooling to room temperature
- filtrationthe precipitate was filtered off with suction
Quellen und Nachweise
- ORD-Eintrag
- ord-02347f89e7ff45a3bdaa4e3d85527075
- Quelldatensatz
- uspto-grants-2008_07
- Patentnummer
- US07402674B2
Verknüpfte Notizen
Wird geladen…