Durch Reaktion des Benzylidentyramins (I) mit Na‐äthylat und nachfolgend den Alkyljodiden (II) in Äthanol bei 50‐80°C (im Falle des Methyljodids bei 25°C) erhält man bei anschließender Verseifung der Azomethine (IIDin50%igem w äßrigenHCl bei 60°C die O‐Alkyl‐tyramine (IV).
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