Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:14]=[CH:15][CH:16]=1)[CH:6]=[N:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[C:17]1(=[O:23])[O:22][C:20](=[O:21])[CH2:19][CH2:18]1>C1(C)C(C)=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]2[CH:19]([C:20]([OH:22])=[O:21])[CH2:18][C:17](=[O:23])[N:7]2[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:14]=[CH:15][CH:16]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 42.3 gm. of 3-methoxybenzylidenaniline, 20 gm. of succinic anhydride and 200 ml. of xylene was refluxed for 16 hours. The crude product was obtained as a solid via the same workup used for example 1B. Recrystallization from ethyl acetate followed by a second recrystallization from acetonitrile provided 21.0 gm. of colorless crystals, m.p. 145°-149°.
Quellen und Nachweise
- ORD-Eintrag
- ord-2259a90d617640fcba2f3dbd82c200ec
- Quelldatensatz
- uspto-grants-1987_01
- Patentnummer
- US04639529
Verknüpfte Notizen
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