The formation of diazonium salts from the corresponding primary aromatic amines and their reaction with potassium iodide to give the corresponding aryl iodide have been performed in a CO2/H2O solvent system. The weak acidity of this system (pH about 3) allowed the formation of triazenes as an intermediate via a reversible reaction. Furthermore, several aryl iodides have been synthesised with high purity. Their isolation was achieved by venting CO2, without the utilization of organic solvents.
No takes yet. Share an insight, caveat, or question.
Tundo et al. (2007) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: