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Esterification of atopic acid and 1-butanol catalyzed by SO3H-functionalized ionic liquid

机译:SO3H官能化离子液体催化特应酸和1-丁醇的酯化

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Several SO_3H-functionalized acidic ionic liquids (ILs) were synthesized by two-step method, using 1, 3-propane sulfone and 1, 4-Butanesultone as raw materials, respectively. It is noteworthy that the ionic liquid using 2-ethyl-4-methylimidazole as source has not been reported. Esterification of 1-butanol with atopic acid was carried out by using these different Bronzed acidic ionic liquids as catalysts. The relationship between the Bronzed acidity-catalytic activity and the relative acidity was studied. Their thermal stability, structure and acidity were characterized by TG-DTG, NMR, UV, respectively. Moreover, the reaction conditions of reaction temperature, molar ratio of reactants, reaction time and ionic liquid amount were optimized. The results indicated that, [2,4-EmiN(CH_2)_4SO_3H][HSO_4] acidic ionic liquid was the best catalyst, and under the optimized reaction conditions of 110°C, n(1-butanol): n(atopic acid)=6:1, m(cat): m(atopic acid)=1.5 %, 3 h, the conversion of atopic acid was 90 % without water-carrying agent.
机译:通过两步法,使用1,3-丙烷砜和1,4-丁烷酮作为原料合成几种SO_3H官能化酸性离子液体(ILS)。值得注意的是,尚未报道使用2-乙基-4-甲基咪唑作为源的离子液体。通过使用这些不同的古铜酸性离子液作为催化剂来进行1-丁醇的酯化。研究了烫金酸度 - 催化活性与相对酸度之间的关系。它们的热稳定性,结构和酸度分别以TG-DTG,NMR,UV为特征。此外,优化了反应温度,反应物的摩尔比,反应时间和离子液体量的反应条件。结果表明,[2,4- emin(CH_2)_4SO_3H] [HSO_4]酸性离子液体是最佳催化剂,并且在110℃的优化反应条件下,N(1-丁醇):N(特应酸) = 6:1,M(猫):M(特特酸)= 1.5%,3小时,特特酸的转化率为90%,无携带剂。

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