研究简报

1,3,5,7-四异氰氧基乙基-1,3,5,7-四甲基环四硅氧烷合成及结构表征

  • 吴林 ,
  • 臧雄 ,
  • 阎四海 ,
  • 唐松青 ,
  • 李战雄
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  • a 苏州大学纺织与服装工程学院 苏州 215021;
    b 中国科学院上海有机化学研究所 上海 200032

收稿日期: 2013-08-27

  修回日期: 2013-10-23

  网络出版日期: 2013-11-05

基金资助

国家自然科学基金(No. 51273140)资助项目.

Synthesis and Characterization of 1,3,5,7-Tetraisocyanatoethyl-1,3,5,7-tetramethylcyclotetrasiloxane

  • Wu Lin ,
  • Zang Xiong ,
  • Yan Sihai ,
  • Tang Songqing ,
  • Li Zhanxiong
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  • a College of Textile and Clothing Engineering, Soochow University, Suzhou 215021;
    b Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032

Received date: 2013-08-27

  Revised date: 2013-10-23

  Online published: 2013-11-05

Supported by

Project supported by the National Natural Science Foundation of China (No. 51273140).

摘要

以丙烯酸和1,3,5,7-四甲基环四硅氧烷(D4H)等为初始原料,经酯化、硅氢加成反应制得1,3,5,7-四(三甲基硅氧羰丙基)-1,3,5,7-四甲基环四硅氧烷(2),水解2制得1,3,5,7-四羧丙基-1,3,5,7-四甲基环四硅氧烷(3),3经Staudinger反应和Curtius重排反应制得1,3,5,7-四异氰氧基乙基-1,3,5,7-四甲基环四硅氧烷(4). 反应总收率为14.5%,化合物结构经1H NMR,29Si NMR,IR,MS和HRMS确证.

本文引用格式

吴林 , 臧雄 , 阎四海 , 唐松青 , 李战雄 . 1,3,5,7-四异氰氧基乙基-1,3,5,7-四甲基环四硅氧烷合成及结构表征[J]. 有机化学, 2014 , 34(3) : 596 -599 . DOI: 10.6023/cjoc201308024

Abstract

1,3,5,7-Tetra(trimethylsiloxysilicatecarboxypropyl)-1,3,5,7-tetramethylcyclotetrasiloxane (2) was prepared by esterification and hydrosilylation reaction using acrylic acid and 1,3,5,7-tetramethylcyclotetrasiloxane (D4H) as raw materials. 2 was hydrolyzed to obtain 1,3,5,7-tetracarboxypropyl-1,3,5,7-tetramethylcyclotetrasiloxane (3) followed by Staudinger reaction and Curtius rearrangement reaction to give 1,3,5,7-tetraisocyanatoethyl-1,3,5,7-tetramethylcyclotetrasiloxane (4) with the total yield of 14.5%. The structure of cyclosiloxane was characterized by 1H NMR, 29Si NMR, IR, MS and HR-MS techniques.

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