This is the polymerization of an amine and an acyl chloride. Acyl chlorides are fairly reactive with primary amines and thus this reaction will
probably happen in fairly light conditions. When this reaction progresses HCl will be given off. This is similar to a condensation reaction where H2O
is released. From what a quick google search showed me, pyridine is often used as a solvent for this reaction to scavenge for free hydrogen, however I
do not know if pyridine is necessary.
Once the larger monomer is formed, a simple connection reaction takes place. This link here might help. http://chemistry2.csudh.edu/rpendarvis/carboxder.html
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