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A practical, efficient, and operationally simple strategy for the ipsoiododecarboxylation and  di -iodination of aromatic carboxylic acids using the low-cost commercial reagent succinimide (NIS) as iodine source is reported. This iodination or  di -iodination process can be easily controlled through reaction conditions, thereby providing corresponding iodination or  di -iodination products with high yields. Furthermore, these two reactions can be easily scaled up to gram-scale by using palladium catalyst (0.66 mol%), which provides high isolated yield.

Simple, Efficient and Controllable Synthesis of Iodo/Di-iodoarenes via Ipsoiododecarboxylation/Consecutive Iodination Strategy