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Oxidation of 2-Acetoxytoluene with Ozone in Acetic Anhydride

机译:乙酸酐中臭氧对2-乙酰氧基甲苯的氧化

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摘要

Kinetics and mechanism of the reaction of ozone with 2-acetoxytoluene in acetic anhydride in the presence of sulfuric acid were studied. It was shown that the prevailing reaction route under these conditions is ozonolysis (89%), and the selectivity of the oxidation of the substrate by the methyl group is no higher 9%. However, in the presence of manganese(II) sulfate as a catalyst, the selectivity increases to 76%. The major reaction products were 2-acetoxybenzyl acetate (59%) and 2-acetoxybenzylidene diacetate (17%). In the presence of a manganese bromide catalyst, the oxidation depth increases, and the major reaction product is already 2-acetoxybenzylidene (66%), while the yield of 2-acetoxybenzyl acetate is 15%. The mechanism of the redox catalysis is considered, that explains the experimental results.
机译:研究了在硫酸存在下臭氧与2-乙酰氧基甲苯在乙酸酐中反应的动力学和机理。结果表明,在这些条件下,主要的反应途径是臭氧分解(89%),并且底物被甲基氧化的选择性不高于9%。然而,在硫酸锰(II)作为催化剂的存在下,选择性增加到76%。主要反应产物是乙酸2-乙酰氧基苄基酯(59%)和2-乙酰氧基苄叉基二乙酸酯(17%)。在溴化锰催化剂的存在下,氧化深度增加,并且主要反应产物已经是2-乙酰氧基亚苄基(66%),而乙酸2-乙酰氧基苄基的产率为15%。考虑了氧化还原催化的机理,解释了实验结果。

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