The study is aimed at the selective synthesis of monoimines from camphor and aliphatic diamines. Three diamines were selected: 1,2-diaminoethane, 1,3-diaminopropane and 1,6-diaminohexane, the latter providing the highest selectivity (over 90%) at a 5-fold molar excess. Comparative analysis showed that the selectivity for 1,6-diaminohexane and 1,3-diaminopropane remains high, whereas for 1,2-diaminoethane it decreases to 77.4%, which is well explained by the reaction mechanism of the studied catalyzed by zinc carboxylates.
D.M. Zapravdina (Wed,) studied this question.