Synthesis of 2,6-Di-tert-butylanthraquinone Cyclically Catalyzed by Brønsted Acidic Ionic Liquids

被引:2
|
作者
Wu, Hujian [1 ]
Wang, Qi [1 ]
Zhang, Xiaoxin [2 ]
Wang, Tao [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem, Dept Organ Chem, Beijing 100029, Peoples R China
[2] Hina Petr & Chem Corp, Inst Petrochem Sci, Beijing 100083, Peoples R China
关键词
SELECTIVE OXIDATION; HYDROGEN-PEROXIDE; ANTHRACENE; ANTHRAQUINONE; DERIVATIVES; ALKYLATION; RADICALS;
D O I
10.1021/acs.iecr.3c02423
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Alkyl anthraquinones play a crucial role as chemical raw materials in the production of hydrogen peroxide as well as intermediates for the synthesis of drugs and dyes. This study focuses on investigating the oxidation reaction of 2,6-di-tert-butylanthracene with hydrogen peroxide, employing Bronsted acidic ionic liquids as catalysts. The optimization of both the anion and cation components within the Br & oslash;nsted acidic ionic iquids was carried out, revealing that bis(3-propanesulfonic acid-1-imidazole)propylidene bisulfate ([2(Im-PS)-C-3][2HSO(4)]) exhibited the most effective catalytic performance. Furthermore, the Br & oslash;nsted acidic ionic liquids demonstrated cyclic catalytic activity during the oxidation reaction. Successful preparation of 2,6-di-tert-butylanthraquinone was achieved with a remarkable yield of up to 92%. The recyclability of the ionic liquid suggests that this study will contribute to technical improvements in the original method while concurrently reducing the cost associated with the synthesis of alkyl anthraquinones via the oxidation method.
引用
收藏
页码:18263 / 18270
页数:8
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