2-Methyl-4-arylthiazole analogues are important intermediates for making photoelectric functional materials.In this paper two kinds of bromine substituted compounds of 2-methyl-4-arylthiazole analogues at 2methyl position and 5-carbon position,respectively,were prepared.The product structures were confirmed by 1HNMR spectrometry.Finally,the mechanisms and conditions of the bromination reactions were analyzed.

This study successfully prepared bromine substituted compounds of 2-methyl-4-arylthiazole analogues at 2methyl and 5-carbon positions, providing valuable intermediates for photoelectric functional materials.

Paper

Study on the bromination reaction of 2-methyl-4-arylthiazole

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