Acetic Anhydride → HCID 21281019, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[O:12][CH3:13].[C:14](OC(=O)C)(=[O:16])C>C(O)=O>[CH3:13][O:12][C:3]1[CH:4]=[C:5]([CH:6]=[O:7])[CH:8]=[C:9]([O:10][CH3:11])[C:2]=1[NH:1][CH:14]=[O:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 10 °C
Versuchsvorschrift
A solution (cooled to 10° C.) of 18.1 g. of 4-amino-3,5-dimethoxy-benzaldehyde in 210 ml. of 98% formic acid was treated dropwise with 70 ml. of acetic anhydride with stirring and the temperature was maintained below 15° C. The solution was then stirred for 2 hours at room temperature, treated with 80 ml. of water and evaporated to dryness under vacuum. The residue was washed with water, recrystallized from alcohol and there was obtained 2',6'-dimethoxy-4'-formyl-formanilide having a melting point of 159°-160° C.
Aufarbeitung
- temperaturethe temperature was maintained below 15° C
- additiontreated with 80 ml
- customof water and evaporated to dryness under vacuum
- washThe residue was washed with water
- customrecrystallized from alcohol
Quellen und Nachweise
- ORD-Eintrag
- ord-f261717c2b9342afb6bf6a2ceb778849
- Quelldatensatz
- uspto-grants-1988_12
- Patentnummer
- US04792557
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