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trimethyl[2-(2-propen-1-yl)octyl]silane | 165059-56-3

中文名称
——
中文别名
——
英文名称
trimethyl[2-(2-propen-1-yl)octyl]silane
英文别名
Trimethyl(2-prop-2-enyloctyl)silane;trimethyl(2-prop-2-enyloctyl)silane
trimethyl[2-(2-propen-1-yl)octyl]silane化学式
CAS
165059-56-3
化学式
C14H30Si
mdl
——
分子量
226.478
InChiKey
ZQZCDFSHKAZBDC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.49
  • 重原子数:
    15
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    辛烯烯丙基三甲基硅烷 在 H+-montmorillonite 作用下, 以 甲苯 为溶剂, 反应 1.0h, 以55%的产率得到trimethyl[2-(2-propen-1-yl)octyl]silane
    参考文献:
    名称:
    Heterogeneous Allylsilylation of Aromatic and Aliphatic Alkenes Catalyzed by Proton-Exchanged Montmorillonite
    摘要:
    Allylsilylation of an alkene is the only known procedure to install both silyl and allyl groups onto a carbon-carbon double bond directly. Proton-exchanged montmorillonite showed excellent catalytic performances for the allylsilylation of alkenes. For example, the reaction of p-chlorostyrene with allyltrimethylsilane proceeded smoothly to afford the corresponding allylsilylated product in 95% yield. We also attempted to Isolate the reaction Intermediate on the montmorillonite surface to Investigate the reaction mechanism,
    DOI:
    10.1021/ol100228t
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文献信息

  • Allylsilylation of alkenes catalyzed by H + -exchanged montmorillonite with water
    作者:Ken Motokura、Shigekazu Matsunaga、Hiroto Noda、Akimitsu Miyaji、Toshihide Baba
    DOI:10.1016/j.cattod.2013.09.058
    日期:2014.5
    Proton-exchanged montmorillonite (H+-montmorillonite) was found to be a heterogeneous catalyst for allylsilylation of alkenes with allylsilanes. A wide variety of aromatic and aliphatic alkenes were effectively converted to the corresponding allylsilylated products in 15-120 min at 60-100 degrees C using H+-montmorillonite with ca. 1-2 wt% of water. The increasing of the amount of water drastically accelerated the allylsilylation of alkenes. For example, the reaction of p-chlorostyrene with allyltrimethysilane afforded 90% yield of the product for 15 min at 40 degrees C using H+-montmorillonite with 8.8 wt% of water, whereas only 2% yield of the product was obtained with 1.3 wt% of water. However, the final product yields with H+-montmorillonite with 1-2 wt% of water were higher than that with the 8.8 wt% of water. A reaction mechanism including the formation of a disilylpropyl cation was proposed. One possible explanation for the role of water is stabilization of the active disilylcation on the montmorillonite surface and/or edges via electron donation from water molecules. (C) 2013 Elsevier B.V. All rights reserved.
  • Heterogeneous Allylsilylation of Aromatic and Aliphatic Alkenes Catalyzed by Proton-Exchanged Montmorillonite
    作者:Ken Motokura、Shigekazu Matsunaga、Akimitsu Miyaji、Yasuharu Sakamoto、Toshihide Baba
    DOI:10.1021/ol100228t
    日期:2010.4.2
    Allylsilylation of an alkene is the only known procedure to install both silyl and allyl groups onto a carbon-carbon double bond directly. Proton-exchanged montmorillonite showed excellent catalytic performances for the allylsilylation of alkenes. For example, the reaction of p-chlorostyrene with allyltrimethylsilane proceeded smoothly to afford the corresponding allylsilylated product in 95% yield. We also attempted to Isolate the reaction Intermediate on the montmorillonite surface to Investigate the reaction mechanism,
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