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The general procedure for the synthesis of 2-fluoro-5-iodonitrobenzene from 1-fluoro-2-nitrobenzene is as follows: Intermediate Example 3. Synthesis of 1-fluoro-4-iodo-2-nitrobenzene To a solution of trifluoromethanesulfonic acid (15.6 ml, 177.15 mmol, 5 eq.) of 1-fluoro-2-nitrobenzene (5 g, 35.43 mmol) was added N-iodosuccinimide (9.57 g, 42.5 mmol, 1.2 eq.) in one batch at 0 °C. The reaction mixture was stirred at room temperature for 1 hour. After completion of the reaction, the reaction was quenched by addition of water and extracted with diethyl ether (3 x 150 ml). The organic layers were combined and washed sequentially with water, aqueous sodium thiosulfate and brine and then dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and the crude product obtained was purified by column chromatography (60-120 mesh silica gel, 5% ethyl acetate in hexane solution as eluent) to afford the target compound 1-fluoro-4-iodo-2-nitrobenzene in 66% yield (6.2 g). 1H NMR (300 MHz, DMSO-d6): δ 8.42 (dd, 1H), 8.18-8.13 (m, 1H), 7.46-7.39 (m, 1H).