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α-呋喃丙烯酸合成工艺改进
The Improved Process for Synthesis of 3-(2-Franyl) acrylic Acid
【摘要】 苯胺在糖醛和丙二酸的Knoevenagel反应中有较好的催化活性。在反应中加入稀释剂苯,可提高收率6%。实验确定的优化条件如下:丙二酸∶糠醛∶苯胺∶吡啶∶苯=1.1∶1 0∶0 1∶2 2∶2 0(mol),反应温度95℃,反应时间3h。优化条件下α 呋喃丙烯酸的收率为98%。稀释剂苯回收率约为95%。
【Abstract】 Aniline had good catlaytic performance in Knoevenagel condensation of furfural with malonic acid.Benzene was used as diluent, and the yield was increased 6%.The premium conditions were determined as folowing:the molar ratio of raw material is malonic acid∶furfural∶aniline∶pyridine∶benzene=1.1∶1.0∶0.1∶2.2∶2.0,reaction temperature 95?℃,reaction time 3?h.In the conditions, the yield of 3-(2-franyl) acrylic acid is 98%.Benzene could be recovered,and the recovery of benzene is about 95%.
【关键词】 α-呋喃丙烯酸;
糠醛;
丙二酸;
苯胺;
苯;
Knoevenagel缩合反应;
【Key words】 3-(2-franyl)acrylic acid; furfural; malonic acid; aniline; benzene; knoevenagel condensation;
【Key words】 3-(2-franyl)acrylic acid; furfural; malonic acid; aniline; benzene; knoevenagel condensation;
- 【文献出处】 精细化工中间体 ,Fine Chemical Intermediates , 编辑部邮箱 ,2004年04期
- 【分类号】TQ251.1
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