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Tetraphenylporphyrin can be synthesized through a modified Rothemund reaction, where 4 equivalents of benzaldehyde are reacted with pyrrole in the presence of a Lewis acid catalyst (such as BF3) and a weak acid like acetic acid. This reaction forms a porphyrinogen intermediate, which is then oxidized to tetraphenylporphyrin using an oxidizing agent like DDQ (2,3-dichloro-5,6-dicyano-1,4-benzoquinone).

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Related Questions

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What has the author Samuel D Bernal written?

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