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

两种新型光敏剂吖啶酮类化合物的合成
引用本文:朱丹,张育川,曾宪玉.两种新型光敏剂吖啶酮类化合物的合成[J].北京化工大学学报(自然科学版),2000,27(2):15-17.
作者姓名:朱丹  张育川  曾宪玉
作者单位:北京化工大学材料科学与工程学院,北京 100029
摘    要:以苯胺类化合物为原料,先后以邻氯苯甲酸和碘苯为烷基化试剂进行了N 烷基化反应,再用浓硫酸使其环化制得N-苯基吖啶酮和3-乙氧基-N-苯基吖啶酮,并用红外光谱及质谱仪检测了各中间体及目标产物的结构。结果表明,当以对乙氧基苯胺为原料时,其第二步反应温度需比以苯胺为原料时降低70~80℃才能得到目标产物;第三步2-羧基-4'-乙氧基三苯胺脱水环化生成了3-乙氧基-N-苯基吖啶酮。

关 键 词:吖啶酮衍生物  光敏剂  烷基取代  吖啶酮衍生物    光敏剂    烷基取代
收稿时间:1999-07-09

Synthesis of two new type photosensitive acridone compounds
ZHU Dan,ZHANG Yu,chuan,ZENG Xian,yu,SHANG Chun,hua.Synthesis of two new type photosensitive acridone compounds[J].Journal of Beijing University of Chemical Technology,2000,27(2):15-17.
Authors:ZHU Dan  ZHANG Yu  chuan  ZENG Xian  yu  SHANG Chun  hua
Institution:College of materials Science and Engineering; Beijing University of Chemiecal Technology, Beijing 100029, China
Abstract:Aniline compounds are used as raw material and reacted with anthranilic acid and then phenyl iodide as alkylating agents to give alkylating products followed by cyclizing with concentrated sulphuric acid to give a N-phenyl-acridone(or 3-ethoxyl-N-phenylacridone).The structure of intermediate and target compound are determined by IR and MS.The results show that using p-ethoxylaniline instead of aniline in the second step reaction, the reaction leads to lower temperature 70~80 ℃ to give target compound. In the third step , dehydrating cyclization of 2-carboxyl-4'-ethoxylt riphenylamine result s in 3-ethoxyl-N-phenylacridone.
Keywords:acridone derivative  photosensitizer  alkylation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《北京化工大学学报(自然科学版)》浏览原始摘要信息
点击此处可从《北京化工大学学报(自然科学版)》下载免费的PDF全文
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