3-(2-Oxo-1,2,3,4-tetrahydroquinolin-3-yl)propanoic acid → HCID 13519806, Verbindung
Reaktionsgleichung
[O:1]=[C:2]1[CH:11](CCC(O)=O)[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[NH:3]1>C(OC(=O)C)(=O)C>[CH2:10]1[C:9]2=[CH:8][CH:7]=[CH:6][C:5]3=[C:4]2[N:3]([C:2](=[O:1])[CH2:11][CH2:10]3)[C:2](=[O:1])[CH2:11]1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
1,2,3,4-Tetrahydro-2-oxo-3-quinolinepropanoic acid (2.1 g, 0.0096 mole) is dissolved in acetic anhydride (10 ml) and the solution is heated to 100° C. for one hour. Excess acetic anhydride is removed at reduced pressure and the residual anhydride is removed by addition of toluene and repeated concentration. The solid is recrystallized from ethyl acetate to yield pure 1,2,6,7-tetrahydro-3H,5H-benzo[ij]quinolizine-3,5-dione, mp 136°-140° C.
Aufarbeitung
- customExcess acetic anhydride is removed at reduced pressure
- customthe residual anhydride is removed by addition of toluene
- concentrationconcentration
- customThe solid is recrystallized from ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-f519d34ee95c48e08da8237f2541d28e
- Quelldatensatz
- uspto-grants-1987_06
- Patentnummer
- US04677112
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