The invention discloses 1, 2-dibromo-6-tert-butyl-9-(4-tert-butylphenyl)-9H-
carbazole and a synthesis method of the 1, 2-dibromo-6-tert-butyl-9-(4-tert-butylphenyl) The method comprises the following steps: taking 3-nitrophthalic acid as an initial
raw material, reacting
trichloroisocyanuric acid with liquid
bromine to obtain 1, 2-dibromo-3-
nitrobenzene, reducing by stannous
chloride to obtain 2, 3-dibromoaniline, carrying out diazotization reaction to obtain 2, 3-dibromophenylhydrazine, reacting with p-tert-butyl
cyclohexanone, and reacting by using 2, 3-dichloro-5, 6-dibromophenylhydrazine to obtain 2, 3-dibromophenylhydrazine. The preparation method comprises the following steps: carrying out
dehydrogenation on 2, 6-dicyanobenzoquinone to obtain 1, 2-dibromo-6-tert-butyl-9H-
carbazole, and finally reacting the 1, 2-dibromo-6-tert-butyl-9H-
carbazole with 4-tert-butyl
iodobenzene to obtain the 1, 2-dibromo-6-tert-butyl-9-(4-tert-butylphenyl)-9H-carbazole. Due to the existence of a
bromine atom functional group on the 1, 2-dibromo-6-tert-butyl-9-(4-tert-butylphenyl)-9H-carbazole, the further conversion of the compound has expandability, and the compound can be used as a material /
drug molecule precursor in the fields of organic light-emitting semiconductors, pharmaceutical
chemistry and the like.