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Synthesis of 1, 2-Aceanthrylenedione Catalyzed by Anhydrous AICl_3

机译:无水AICl_3催化合成1,2-乙二基二酮。

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摘要

1,2-aceanthrylenedione was synthesized through the acylation reaction of anthracene and oxalyl chloride catalyzed by anhydrous AlCl_3. The effects of various reaction conditions on the yield and selectivity of 1, 2-aceanthrylenedione were studied by GC analysis. The results show that the optimum synthesis conditions of the acylation reaction are as follows : the molar ratio of oxalyl chloride to anthracene being 1:2, the molar ratio of anhydrous AlCl_3 to anthracene being 4:1, the reaction time being 5 h, the reaction temperature being 303k and the solvent of the reaction system being CS_2. Under those conditions, the yield and selectivity of 1, 2-aceanthrylenedione is 83.8 % and 92.3% respectively. Pure 1, 2-aceanthrylenedione was prepared by extraction and recrystallation. The structure of 1, 2-aceanthrylenedione was identified by measure of melting point, GC/MS, FTIR and ~1HNMR analyses.
机译:通过无水AlCl_3催化蒽与草酰氯的酰化反应合成了1,2-乙二酮。通过GC分析研究了各种反应条件对1,2-乙二酮的收率和选择性的影响。结果表明,酰化反应的最佳合成条件为:草酰氯与蒽的摩尔比为1:2,无水AlCl_3与蒽的摩尔比为4:1,反应时间为5 h,反应温度为303k,反应体系的溶剂为CS_2。在这些条件下,1,2-乙撑二酮的产率和选择性分别为83.8%和92.3%。通过萃取和重结晶制备纯的1,2-乙撑二酮。通过测量熔点,GC / MS,FTIR和〜1HNMR分析确定1,2-乙二酮的结构。

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