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苯甲酸与乙二胺反应的研究
引用本文:徐家业,何力,王晓玲,张群正,尹晓红.苯甲酸与乙二胺反应的研究[J].西安石油大学学报(自然科学版),2001,16(1):40-42.
作者姓名:徐家业  何力  王晓玲  张群正  尹晓红
作者单位:西安石油学院 化学工程系,
摘    要:在不同条件下考察了苯甲酸与乙二胺的反应 ,对反应产物、主要副产物及反应中间体进行了分离和鉴定 ,通过熔点测定、元素分析和红外光谱分析 ,确定了产物为 2 -苯基咪唑啉 ,主要副产物为二苯甲酰乙二胺 ,中间体之一为乙二胺与苯甲酸形成的双盐 .试验发现在不同溶剂中反应的产物和副产物的比例 ,产物纯度相差很大 .对反应机理及溶剂效应进行了讨论 .

关 键 词:咪唑啉  表面活性剂  苯甲酸  乙二胺  鉴定
文章编号:1001-5361(2001)01-0040-03
修稿时间:2000年4月19日

Studies on the Reaction of Benzoic Acid and Ethylenediamine
XU Jia ye,HE Li,WANG Xiao ling,et al.Studies on the Reaction of Benzoic Acid and Ethylenediamine[J].Journal of Xian Shiyou University,2001,16(1):40-42.
Authors:XU Jia ye  HE Li  WANG Xiao ling  
Abstract:The reaction of benzoic acid and ethylenediamine was studied under different conditions. The product, chief byproduct and one of the intermediates of the reaction were separated and identified. It was found that their yields depend on the solvents used in the reaction. According to melting point, elementary analysis, NMR, and IR spectrum, it is known that the product is 2-phenylimidazoline[m.p.:98.5~100.5℃;elementary analysis(%) calcd.:C 73.97, H6.85, N 19.18, Measured: C 73.89, H6.89, N18.89;IR(KBr):υ/cm-13200(NH),1612 (C=N),1600 (benzene ring), 782 and 698 (monosubsd. ofbenzene ring); 1H NMR (90 MHz), δ:3.70(s.4H,CH2CH2),5.18~5.43(br,1 H,NH),7.17~7.90(m,5H,C6H5)], the chief byproduct is dibenzoylethylenediamine[m.p.:247.5~248.5℃(249[4]);IR(KBr):υ/cm-1 3300 (NH), 1634(C=O),1606(benzene ring),1556(amide Ⅱ band),same as Sadtler standard spectrum of No.3342,1980)],and the intermediate is the salt of benzoic acid with ethylenediamine[m.p.:151.0~153.0℃;elementary analysis(%)calcd.:C 63.16,H6.58,N9.21, measured: C63.23, H6.75, N8.90;IR(KBr):υ/cm-1]3000(br,NH+3 CH), 2172(NH+3,couple vibration),1630(C=O),1598(benzene ring),1386(s,COO )].The reaction mechanism was also discussed.
Keywords:imidazoline  surfactant  benzoic acid  ethylenediamine  identification
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