Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([OH:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.CC(C)[O-].[Al+3:24].CC(C)[O-].CC(C)[O-].O>C(O)(C)C>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.[Al+3:24].[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2.5 G of 2-(5H-[1]benzopyrano[2,3-b]pyridin-7-yl)propionic acid is dissolved in 80 ml of isopropyl alcohol. A solution of 2.1 g of aluminum isopropoxide in 25 ml of isopropyl alcohol is added dropwise to the solution with stirring, white crystals being immediately yielded. After refluxing the mixture for 1 hour, 3 ml of water is added, and then the whole mixture is further refluxed for 1 hour. After cooling, the crystals are filtered off, washed with isopropyl alcohol, and dried to give aluminum 2-(5H-[1]-benzopyrano[2,3-b]pyridin-7-yl)propionate as white crystals melting at above 250°C.
Aufarbeitung
- customwhite crystals being immediately yielded
- temperatureAfter refluxing the mixture for 1 hour
- temperaturethe whole mixture is further refluxed for 1 hour
- temperatureAfter cooling
- filtrationthe crystals are filtered off
- washwashed with isopropyl alcohol
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-046c44be7a3645999781925f225f62a5
- Quelldatensatz
- uspto-grants-1976_01
- Patentnummer
- US03931205
Verknüpfte Notizen
Wird geladen…