Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:13][CH2:14][NH2:15])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].[C:16](OC(=O)C)(=[O:18])C>C(O)=O>[CH:16]([CH:13]([C:5]1[CH:6]=[C:7]([O:11][CH3:12])[C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=1)[CH2:14][NH2:15])=[O:18]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1.422 kg of 3,4,5-trimethoxy-phenylethylamine is slowly added to a mixture of 2.185 kg of 98% formic acid and 1.728 kg of acetic anhydride, while maintaining the temperature at about 50°. The reaction bath is maintained at this temperature for about 3 hours and the formic acid and acetic acid mixture and the excess anhydride is distilled. The formylated derivative thus obtained (1.734 kg) is used unpurified.
Aufarbeitung
- temperaturewhile maintaining the temperature at about 50°
- temperatureThe reaction bath is maintained at this temperature for about 3 hours
- distillationthe formic acid and acetic acid mixture and the excess anhydride is distilled
- customThe formylated derivative thus obtained (1.734 kg)
Quellen und Nachweise
- ORD-Eintrag
- ord-19c0d8cc26114b74b636f14f770ebde7
- Quelldatensatz
- uspto-grants-1981_11
- Patentnummer
- US04302458
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