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Synthesis of 8-bromo-5,12-tetracenequinone and 2-bromotetracene derivatives

机译:8-溴-5,12-并四苯醌和2-溴并四苯衍生物的合成

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摘要

A series of bromotetracenequinones 1 and bromotetracenes 2 were prepared from 4-bromophthalic anhydride. The parent tetracenequinone 1a and tetracene 2a were sparingly soluble in organic solvents. In contrast, dipropyl-substituted tetracenequinone 1b and tetracene 2b were a little more soluble. Preparation of dihexyl-substituted tetracene 2c proved to be difficult. Sonogashira coupling of 1b with trimethylsilylacetylene afforded the corresponding product.
机译:由4-溴邻苯二甲酸酐制备了一系列的溴四并苯醌1和溴代四氢呋喃酮2。母体并四苯醌1a和并四苯2a微溶于有机溶剂。相反,二丙基取代的并四苯醌1b和并四苯2b的溶解性稍高。证明制备二己基取代的并四苯2c是困难的。 1b与三甲基甲硅烷基乙炔的Sonogashira偶联得到相应的产物。

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