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非重氮化法合成偶氮化合物1,2,3,4,5,6-三(4-偶氮苯基)苯

Synthesis of 2,6,10-tris(phenylazo)-1,2,3,4,5,6,7,8,9,10,11,12-dodecahydrotriphenylene by a non-diazotization method
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摘要 本实验通过基础原料苯肼和1,4-环己二酮合成了1,4-环己二酮单苯腙(1),(1)在乙醇和二氯亚砜作用下三聚芳构化得到了1,2,3,4,5,6-三(4-偶氮苯基)苯(2),从而通过重氮化法合成了一种新型的偶氮化合物.该法操作简单,对环境友好,为生产偶氮化合物提供了新的途径. 4-(phenyl-hydrazono)-cyclohexanone (1) was synthesized from phenylhydrazine and 1,4-cyclohexanedione. 2,6, 10-tris (phenylazo) -1,2,3,4,5,6,7,8,9,10,11,12-dodecahydrotriphenylene (2) was prepared by trimerization and aromatization of 1 in the presence of thionyl chloride in anhydrous ethanol. The new type of azostuff (2) was produced by a non-diazotiation method which was simple and safe to the environment. It provided a new method for the synthesis of azo-compounds.
出处 《天津理工大学学报》 2007年第6期1-2,共2页 Journal of Tianjin University of Technology
基金 国家自然科学基金(G20472064) 天津市自然科学基金(040884311)
关键词 偶氮化合 1 4-环己二酮 苯肼 芳构化 非重氮化法 1 2 3 4 5 6-三(4-偶氮苯基)苯 azo-compound 1,4-cyclohexandione phenylhydrazine aromatization non-diazotiation method 2,6, 10-tris (phenylazo) -1,2,3,4,5,6,7,8,9,10,11,12-dodecahydrotriphenylene
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