功能化离子液体催化合成辛酸苄酯
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O643.3

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国家高技术研究发展计划(863计划)


Synthesis of Benzyl octanoate Catalyzed by Functionalized Ionic Liquids
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    摘要:

    以苯甲醇与正辛酸合成辛酸苄酯为探针反应,咪唑类和吡啶类具有-PS(丙烷磺酸基)功能基团的离子液体作催化剂,考察了其阴阳离子对催化活性的影响。并选择[PSPy]HSO4为催化剂,研究了酸醇比、催化剂用量、反应温度和反应时间等对酯化率的影响,实验结果表明:在酸醇比为1:1.5,催化剂用量为正辛酸的20 mol%,反应温度为120 ℃,酯化率达到95.3%;此外,该催化剂重复使用10次后,活性基本保持不变,酯化率仍有94.2%,显示了高的稳定性和催化活性

    Abstract:

    A series of task-specific ionic liquids (TSILs) with imidazolium and pyridinium that bear an alkane sulfonic acid group were synthesized. The synthesis of benzyl octanoate used benzil alcohol and octanoic acid as reactants and these TSILs as catalyst was investigated. Effect of anion and cation of TSILs on their catalytic performance was also investigated. The results showed that the conversion of octanoic acid reached 95.3% by using [PSPy]HSO4 as catalyst under conditions of n octanoic acid : n benzil alcohol= 1:1.5, 20 mol% of octanoic acid for TSILs, 120℃ and 2.5 h. In addition, the [PSPy]HSO4 exhibited excellent stability and catalytic activity. It could be reused ten times without considerable loss of activity and still had a conversion of 94.2%.

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尹万香,龙俞霖,李润生,杨骏.功能化离子液体催化合成辛酸苄酯[J].精细化工,2010,27(10):

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  • 收稿日期:2010-05-10
  • 最后修改日期:2010-07-08
  • 录用日期:2010-07-20
  • 在线发布日期: 2010-09-07
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