甲吡唑的合成方法
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TQ463.53

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the Synthesis of Fomepizole
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    摘要:

    采用3种方法合成甲吡唑,分别以异丁醛或异丁烯醛为起始原料,与质量分数80%水合肼和浓硫酸在碘化钾催化条件下反应制得。对这三种方法进行工艺优化,探讨加料顺序、溶剂浓度及反应温度对收率的影响。方法(1)以低沸点异丁醛为起始原料,通过改变加料方式,避免使用高压釜,操作简便可行,产率为40%。方法(2)改用异丁烯醛为起始原料,避免异丁醛易挥发的缺点,通过优化反应条件产率可达80%。方法(3)中使用双氧水,操作繁琐,不适用于工业化生产。 结论:方法(2)操作简单易行,且收率较高,为三者中制备甲吡唑的最佳合成方法。

    Abstract:

    In this article, fomepizole was prepared from isobutyraldehyde or 2-methyl-2-propenal in three ways. Both of the starting materials were reacted with 80% hydrazine hydrate (w%), sulfuric acid and potassium iodide. By exploring the influence of adding order, concentration and reaction temperature on the yield, optimize the process. The first process started with isobutyraldehyde, with low boiling point. It was convenient by changing the way of feeding, which can avoid using of autoclave, and the yield was 40%. The second process had been changed to use 2-methyl-2-propenal, avoiding weakness of low boiling point. By optimizing the reaction conditions, the yield can reach to 80%. The third one showed complex operation, with the usage of hydrogen peroxide, which was not suitable for industry. Conclusion: Among those three, the second one, which was operated simply with high yield, was most suitable for industry.

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吕程程.甲吡唑的合成方法[J].精细化工,2015,32(8):

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  • 收稿日期:2015-03-31
  • 最后修改日期:2015-05-13
  • 录用日期:2015-05-25
  • 在线发布日期: 2015-07-07
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