4-[diallyl(ethoxy)silyl]-N,N-diphenylaniline

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 4-[diallyl(ethoxy)silyl]-N,N-diphenylaniline
• 英文别名: N,N-diphenyl-4-(diallylethoxysilyl)aniline；4-[ethoxy-bis(prop-2-enyl)silyl]-N,N-diphenylaniline
• 化学式: C₂₆H₂₉NOSi
• 分子量: 399.608
• InChiKey: RHEVGUPVPCOJFB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.72
• 重原子数：
  29
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-bromo-4-(diallylethoxysilyl)benzene 、 二苯胺 在 tris-(dibenzylideneacetone)dipalladium(0) 、 2-(二叔丁基膦)联苯 sodium t-butanolate 作用下， 以 甲苯 为溶剂， 反应 19.0h， 以62%的产率得到4-[diallyl(ethoxy)silyl]-N,N-diphenylaniline
  参考文献：
  名称：

  Organosilane compound and organosilica obtained therefrom

  摘要：

  提供的有机硅烷化合物可由以下任一通用式（1）至（7）表示：（其中：Ar代表苯基或类似物；R1代表氢原子或类似物；R2至R8分别代表甲基基团或类似物；n表示范围为0至2的整数；m表示1或2的整数；L代表单键或类似物；X代表氢原子或类似物；Y代表氢原子或类似物）。

  公开号：

  US20080227939A1

文献信息

• Organosilane compound and organosilica obtained therefrom
  申请人：Mizoshita Norihiro

  公开号：US20080227939A1

  公开（公告）日：2008-09-18

  Provided is an organosilane compound expressed by any one of the following general formulae (1) to (7): (wherein: Ar represents a phenylene group or the like; R 1 represents a hydrogen atom or the like; R 2 to R 8 each represent a methyl group or the like; n represents an integer in a range from 0 to 2; m represents an integer of 1 or 2; L represents a single bond or the like; X represents a hydrogen atom or the like; and Y represents a hydrogen atom or the like).

  提供的有机硅烷化合物可由以下任一通用式（1）至（7）表示：（其中：Ar代表苯基或类似物；R1代表氢原子或类似物；R2至R8分别代表甲基基团或类似物；n表示范围为0至2的整数；m表示1或2的整数；L代表单键或类似物；X代表氢原子或类似物；Y代表氢原子或类似物）。
• Preparation of functionalized aryl(diallyl)ethoxysilanes and their palladium-catalyzed coupling reactions giving sol–gel precursors
  作者：Yoshifumi Maegawa、Toyohiro Nagano、Tatsuya Yabuno、Hiroki Nakagawa、Toyoshi Shimada

  DOI：10.1016/j.tet.2007.08.011

  日期：2007.11

  A series of molecular building blocks containing allylsilyl groups, which can be incorporated into the appropriate sol-gel precursors as fragments, were prepared. The allylsilyl group is retained unchanged over the course of all reactions giving sol-gel precursors and behave as the synthetic equivalent of alkoxysilyl groups toward sol-gel polymerization, but are stable enough to allow purification by silica gel chromatography. These allylsilanes were successfully used as building blocks to construct functional sol-gel precursors via palladium-catalyzed coupling reactions. (C) 2007 Elsevier Ltd. All rights reserved.