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[3-Cyclohexyl-2-(trimethylsilylmethyl)prop-2-enyl]-trimethylsilane | 928796-03-6

中文名称
——
中文别名
——
英文名称
[3-Cyclohexyl-2-(trimethylsilylmethyl)prop-2-enyl]-trimethylsilane
英文别名
——
[3-Cyclohexyl-2-(trimethylsilylmethyl)prop-2-enyl]-trimethylsilane化学式
CAS
928796-03-6
化学式
C16H34Si2
mdl
——
分子量
282.617
InChiKey
DDBOYLHEPJMJAL-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):
    6.17
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    [3-Cyclohexyl-2-(trimethylsilylmethyl)prop-2-enyl]-trimethylsilane4-甲基苯磺酸吡啶 作用下, 以 四氢呋喃乙腈 为溶剂, 以100%的产率得到(2-(cyclohexylmethyl)allyl)trimethylsilane
    参考文献:
    名称:
    Preparation of 2-trimethylsilylmethyl-1-alkene; cross-coupling and protodesilylation sequence from 1,1-dibromo-1-alkene
    摘要:
    A new method for the preparation of exomethylene type allylsilane is described. Selective mono-protodesilylation of 1-trimethylsityl-2-trimethylsilylmethyl-2-alkenes 2 with PPTS afforded 2-trimethylsilylmethyl-l-alkeiles 4 in excellent yields. Since the resulting allylsilanes 4 possess an exomethylene unit, the reactions of 4 with carbonyl compounds in the presence of Lewis acids gave the corresponding product 7 having an exomethylene unit in excellent yields. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.12.044
  • 作为产物:
    描述:
    1,1-dibromo-2-cyclohexylethene(三甲基硅基)甲基氯化镁 在 palladium diacetate 、 三苯基膦 作用下, 以 四氢呋喃乙醚 为溶剂, 以85%的产率得到[3-Cyclohexyl-2-(trimethylsilylmethyl)prop-2-enyl]-trimethylsilane
    参考文献:
    名称:
    Preparation of 2-trimethylsilylmethyl-1-alkene; cross-coupling and protodesilylation sequence from 1,1-dibromo-1-alkene
    摘要:
    A new method for the preparation of exomethylene type allylsilane is described. Selective mono-protodesilylation of 1-trimethylsityl-2-trimethylsilylmethyl-2-alkenes 2 with PPTS afforded 2-trimethylsilylmethyl-l-alkeiles 4 in excellent yields. Since the resulting allylsilanes 4 possess an exomethylene unit, the reactions of 4 with carbonyl compounds in the presence of Lewis acids gave the corresponding product 7 having an exomethylene unit in excellent yields. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.12.044
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