反-4-(反-4′-正丙基环己基)-环己基甲醛的合成与表征
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Synthesis and characterization of trans-4-(trans-4′-n-propylcyclohexyl)cyclohexyl aldehyde
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    摘要:

    摘要:以反-4-(4′-正丙基环己基)-苯甲醛丙二醇缩醛为起始原料,经加氢、酸解及异构化反应得到纯度98%以上的反-4-(反-4′-正丙基环己基)-环己基甲醛,总收率为39.2%,目标化合物的结构经1HNMR、IR及GC-MS确认。探讨了反-4-(4′-正丙基环己基)-苯甲醛丙二醇缩醛加氢的反应条件,条件实验表明:以钌/碳做催化剂,乙醇做反应溶剂,当m[反-4-(4′-正丙基环己基)-苯甲醛丙二醇缩醛]:m(钌/碳)=1 g : 0.09 g,加氢压力为3.5 MPa,反应温度为35~40 ℃时,反应效果最佳。

    Abstract:

    Abstract:More than 98% purity of trans-4-(trans-4′-n-propylcyclohexyl)cyclohexyl aldehyde was obtained via hydrogenation,acidolysis and isomerization reaction with trans-4-(4′- n-propylcyclohexyl)-benzaldehyde propylene glycolacetal as the starting material, the total yield was 39.2%, the structure of the target compound was confirmed by 1HNMR, IR and GC-MS. The hydrogenation reaction conditions of trans-4-(4′-n-propylcyclohexyl)-benzaldehyde propylene glycolacetal were investigated,the results of the condition experiments showed that the reaction effect was best when Ru/C was as the catalyst, ethanol was as the reaction solvent,m[trans-4-(4′- n-propylcyclohexyl)-benzaldehyde propylene glycolacetal]:m(Ru/C) was 1 g : 0.09 g,the hydrogenation pressure was 3.5 MPa,the reaction temperature was 35~40 ℃.

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王小明.反-4-(反-4′-正丙基环己基)-环己基甲醛的合成与表征[J].精细化工,2014,31(1):

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  • 收稿日期:2013-08-07
  • 最后修改日期:2013-11-03
  • 录用日期:2013-11-05
  • 在线发布日期: 2014-01-03
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