4-Iodo-1,2-dimethylbenzene

• 3-arylacrylamide
• 3,3-diaryl substituted acrylamide
• 3-arylpropylamine
• di-tert-butyl 1-(3,4-dimethylphenyl)hydrazine-1,2-dicarboxylate
• 2,3,7,8-tetramethyldibenzofuran
• N-(3-(3,4-Dimethylphenyl)-2-phthalimidopropionyl)-2-methylthioaniline

95-47-6

31599-61-8

GENERAL STEPS: To a solution of 1,2-dimethylbenzene (o-xylene, 0.106 g, 1 mmol) in acetonitrile (10 mL) was sequentially added iodine (1 mmol, 0.126 g) and polymer-loaded periodate (0.6 g, 1.05 mmol). The reaction mixture was stirred at 40 °C for 1 hour. The progress of the reaction was monitored by thin layer chromatography (TLC) and the unfolding agent was a solvent mixture of ethyl acetate and hexane (1:9, v/v). After completion of the reaction, the mixture was cooled to room temperature and filtered. Excess iodine in the filtrate was removed by adding sodium bisulfite solution (1 M) dropwise. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography, the eluent being a solvent mixture of hexane and ethyl acetate. The final product was 3,4-dimethyl iodobenzene in 95% isolated yield with a boiling point of 235 °C (literature value: 234 °C).