Reaktionsgleichung
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][O:10][C:11]1[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=1[NH2:13]>C1(C)C=CC=CC=1>[CH3:9][O:10][C:11]1[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=1/[N:13]=[CH:1]/[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 31.8 g (0.30 mol) of benzaldehyde, 36.9 g (0.30 g) of 2-methoxyaniline and 450 mL of toluene was refluxed using a Dean-Stark head for 1 hr. 15 granules of 4A molecular sieves were added. This mixture was refluxed for 4 hr, then filtered off, and the filtrate was evaporated to dryness. The residue was dried in vacuum at 70° C. This crude product was further used without an additional purification, since it is unstable on silica gel 60 and decomposes when dried under vacuum. Yield 52.0 g (82%) of the title material.
Aufarbeitung
- temperaturewas refluxed
- customfor 1 hr
- temperatureThis mixture was refluxed for 4 hr
- filtrationfiltered off
- customthe filtrate was evaporated to dryness
- customThe residue was dried in vacuum at 70° C
- customThis crude product was further used without an additional purification, since it
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-c8f4ee2ab0a142a4b1a7590925e67ed8
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08530593B2
Verknüpfte Notizen
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