Abstract
A practical and proecological improvement for synthesis of meso-tetraphenylporphyrin (meso-TPP) under microwave irradiation is described. A cyclocondensation reaction of benzaldehyde and pyrrole followed by oxidation of the porphyrinogen formed as an intermediate in a small amount of propionic acid at 120 °C (under controlled microwave heating) resulted in conversion to meso-TPP in a reasonable yield (ca. 30%) in preparative-scale experiments (300–500 mg). The influence of many parameters such as the concentration of reagents, catalyst, solvent, temperature, reaction time, and oxidant on the reaction yield was studied. The environmental motive in this improvement is reduction of solvent volume (ca. 250 times). Also, some toxic reagents were eliminated from the procedure.
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