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Klaus-Dieter Warzecha
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With excess of methylamine, I wouldn't exclude additional methylation, yielding a trimethylanilinium iodide.

alkylation of dimethylaniline

However, the reaction should stop there since a further hydrogen abstraction from a $\beta$-position isn't possible.

With excess of methylamine, I wouldn't exclude additional methylation, yielding a trimethylanilinium iodide. However, the reaction should stop there since a further hydrogen abstraction from a $\beta$-position isn't possible.

With excess of methylamine, I wouldn't exclude additional methylation, yielding a trimethylanilinium iodide.

alkylation of dimethylaniline

However, the reaction should stop there since a further hydrogen abstraction from a $\beta$-position isn't possible.

Source Link
Klaus-Dieter Warzecha
  • 44.2k
  • 8
  • 104
  • 166

With excess of methylamine, I wouldn't exclude additional methylation, yielding a trimethylanilinium iodide. However, the reaction should stop there since a further hydrogen abstraction from a $\beta$-position isn't possible.