2-(5-Chloro-2-nitrophenoxy)-5-methoxybenzoic acid → 1-Chloro-7-methoxy-4-nitro-9H-xanthen-9-one
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N+:20]([O-:22])=[O:21])=[C:6]([CH:19]=1)[O:7][C:8]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][C:9]=1[C:10]([OH:12])=O>O>[Cl:1][C:2]1[C:19]2[C:10](=[O:12])[C:9]3[C:8](=[CH:16][CH:15]=[C:14]([O:17][CH3:18])[CH:13]=3)[O:7][C:6]=2[C:5]([N+:20]([O-:22])=[O:21])=[CH:4][CH:3]=1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
2-(5-Chloro-2-nitrophenoxy)-5-methoxybenzoic acid, 50 g, was added to 400 g of polyphosphoric acid, and the mixture stirred at 110° C. for 24 hours. The mixture was poured into 2 liters of water, and the resulting precipitate filtered to afford a light green solid. Recrystallization from dimethylformamide gave the title compound as green needles, mo 249°-251° C.
Aufarbeitung
- filtrationthe resulting precipitate filtered
- customto afford a light green solid
- customRecrystallization from dimethylformamide
Quellen und Nachweise
- ORD-Eintrag
- ord-d34880c459dc4c43938c4e920aab3ae5
- Quelldatensatz
- uspto-grants-1986_08
- Patentnummer
- US04604390
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