Abstract
AbstractTo establish appropriate reaction conditions for the synthesis of new monomers having a secondary amino group, a lithium alkylamide catalyzed addition reaction of primary amines with styrene was examined as the model reaction. The selectivity of N‐alkyl‐2‐phenethylamines (2) and the rate constant of the reaction were determined. On the basis of results of the model reaction, new styrene derivatives having a secondary amino group (5) were synthesized by lithium alkylamide catalyzed addition reactions of primary amines with 1,4‐divinylbenzene.
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