首页 | 本学科首页   官方微博 | 高级检索  
     检索      

一个研究型含氟杂环化合物实验的设计
引用本文:蒋海珍.一个研究型含氟杂环化合物实验的设计[J].实验室研究与探索,2011,30(12):97-100.
作者姓名:蒋海珍
作者单位:上海大学理学院化学系,上海20044
基金项目:国家自然科学基金资助项目(20772079,21072127,21032006);上海市科学技术委员会(10JC1405600,08JC1409900);上海市教育委员会项目
摘    要:设计了一个由底物控制的化学选择性合成含氟吡唑、哒嗪酮和吲哚衍生物的实验.此研究型实验是以不同碳链长度的β,γ和δ-含氟酮酸酯为底物与苯肼在对甲苯磺酸的作用下,以甲苯为溶剂一锅反应分别得到具有潜在生理活性的含氟吡唑、哒嗪酮和吲哚衍生物.实验操作简便、反应条件温和.反应的进程可用TLC和19F NMR谱跟踪.产物结构经红外光谱、核磁共振氢谱、氟谱和碳谱及元素分析等表征和确定,对底物控制的化学选择性形成不同的产物进行了分析,并对此研究型实验在实验教学工作中的实践效果进行了探讨.

关 键 词:研究型实验设计  含氟杂环化合物  选择性合成  底物控制  谱图解析

An Exploration-oriented Experimental Design on Chemoselective Synthesis of Fluorinated Heterocycles
JIANG Hai-zhen.An Exploration-oriented Experimental Design on Chemoselective Synthesis of Fluorinated Heterocycles[J].Laboratory Research and Exploration,2011,30(12):97-100.
Authors:JIANG Hai-zhen
Institution:JIANG Hai-zhen(Department of Chemistry,College of Sciences,Shanghai University,Shanghai 200444,China)
Abstract:A simple and facile exploring organic chemistry experiment was designed on a substrate-controlled chemoselective one-pot synthesis of biologically interested trifluoromethylated heterocycles,such as indoles,dihydropyridazinones and pyrazole-3-ol derivatives,through the different chain length of substrates of(-trifluoromethyl substituted(,(,(-ketoesters reacting with phenylhydrazine under the promotion of p-TsOH in the toluene.The experimental results were traced by TLC or 19F NMR,and the structure of the products were analyzed and confirmed by IR,1H NMR,13C NMR,19F NMR and elemental analysis.Plausible reaction pathway from ketoesters to indole or 1,2-diaza-3-one heterocycles was deduceed.Practical effects in the experimental teaching were discussed as well.
Keywords:exploration-oriented experimental design  fluorine-containing heterocycles  chemoselective  substrate-controlled  spectral identification
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号