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tert-butyl(chloro)diethoxygermane | 500372-15-6

中文名称
——
中文别名
——
英文名称
tert-butyl(chloro)diethoxygermane
英文别名
Tert-butyl-chloro-diethoxygermane;tert-butyl-chloro-diethoxygermane
tert-butyl(chloro)diethoxygermane化学式
CAS
500372-15-6
化学式
C8H19ClGeO2
mdl
——
分子量
255.281
InChiKey
UIZPSRWDCLXFBT-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

物化性质

  • 沸点:
    197.2±23.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.04
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    tert-butyl(chloro)diethoxygermane 在 water 作用下, 以 乙醇 为溶剂, 以29.1%的产率得到5,7-dichloro-1,3,5,7,9-hexa-tert-butyltricyclo[7.3.1.1(3,7)]octagermoxane
    参考文献:
    名称:
    Synthesis and characterization of alkylgermasesquioxanes
    摘要:
    Alkyl(chloro)ethoxygermanes, RGe(OEt)(n)Cl3-n (R = i-Pr, n = 0; R = t-Bu, n = 0-3; R = cyclo-C6H11, n = 0) were hydrolyzed with aqueous NaOH in xylene at 130-140 degreesC to give cage hexakis(alkylgermasesquioxane)s, (RGe)(6)O-9. These structures of cage (RGe)(6)O-9 were fully confirmed by spectroscopic and X-ray diffraction methods. t-Butyldichloro(ethoxy)germane, t-BuGe(OEt)Cl-2, was carefully treated with water at 5 degreesC for 3 h to afford cis, trans-1,3,5-tri-t-butyl-1,3,5-trichlorocyclotrigermoxane, (t-BuClGeO)(3). Hydrolysis of (t-BuClGeO)(3) at 5 degreesC for additional 33 h gave a tricyclic anti-form ladder 5,7-dichloro-1,3,5,7,9,1 1-hexat-butyltricyclo[7.3.1.1(3.7)]hexagermoxanes, (t-BuGe)(6)O8Cl2. The tricyclic ladder (t-BuGe)(6)O8Cl2 was also prepared by hydrolysis of t-butyl(chloro)diethoxygermane, t-BuGe(OEt)(2)Cl, at 5 degreesC for 6 It, and its structure was determined by spectroscopic and X-ray diffraction analysis. The tricyclic ladder germoxane reacted with aqueous NaOH in xylene at 130-140 degreesC for 3 h to afford hexakis(t-butylgermasesquioxane), (t-BuGe)(6)O-9. The formation mechanism of the germasesquioxane, (t-BuGe)(6)O-9 from t-butyl(chloro)ethoxygermanes, t-BuGe(OEt)(n)Cl3-n (n = 0-3) is also discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(02)02157-5
  • 作为产物:
    描述:
    乙醇叔丁基-三氯-锗烷 在 C5H5N 作用下, 以 neat (no solvent) 为溶剂, 生成 tert-butyl(chloro)diethoxygermane
    参考文献:
    名称:
    Synthesis of Hexakis(alkylgermasesquioxane)s from Alkyl(chloro)ethoxygermanes and Their Formation Mechanism
    摘要:
    烷基(氯)乙氧基锗烷用水水解得到1,3,5-三烷基-1,3,5-三氯环三锗氧烷。 1,3,5-三氯环三甲氧烷的水解得到5,7-二氯-1,3,5,7,9,11-六烷基三环[7.3.1.13,7]六甲氧烷。三环反式梯形六锗氧烷与水反应得到六(烷基锗倍半氧烷)。这些笼型和梯型锗氧烷通过光谱和X射线衍射方法进行了鉴定。
    DOI:
    10.1246/cl.2002.1124
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文献信息

  • Synthesis of Hexakis(alkylgermasesquioxane)s from Alkyl(chloro)ethoxygermanes and Their Formation Mechanism
    作者:Masato Nanjo、Takaomi Sasage、Kunio Mochida
    DOI:10.1246/cl.2002.1124
    日期:2002.11
    Alkyl(chloro)ethoxygermanes were hydrolyzed with water to give 1,3,5-trialkyl-1,3,5-trichlorocyclotrigermoxanes. Hydrolysis of 1,3,5-trichlorocyclotrigermoxanes gave 5,7-dichloro-1,3,5,7,9,11-hexaalkyltricyclo[7.3.1.13,7]hexagermoxanes. The tricylic anti-form ladder hexagermoxanes reacted with water to afford hexakis(alkylgermasesquioxane)s. These cage and ladder germoxanes were identified by spectrospcopic and X-ray diffraction methods.
    烷基(氯)乙氧基锗烷用水水解得到1,3,5-三烷基-1,3,5-三氯环三锗氧烷。 1,3,5-三氯环三甲氧烷的水解得到5,7-二氯-1,3,5,7,9,11-六烷基三环[7.3.1.13,7]六甲氧烷。三环反式梯形六锗氧烷与水反应得到六(烷基锗倍半氧烷)。这些笼型和梯型锗氧烷通过光谱和X射线衍射方法进行了鉴定。
  • Synthesis and characterization of alkylgermasesquioxanes
    作者:Masato Nanjo、Takaomi Sasage、Kunio Mochida
    DOI:10.1016/s0022-328x(02)02157-5
    日期:2003.2
    Alkyl(chloro)ethoxygermanes, RGe(OEt)(n)Cl3-n (R = i-Pr, n = 0; R = t-Bu, n = 0-3; R = cyclo-C6H11, n = 0) were hydrolyzed with aqueous NaOH in xylene at 130-140 degreesC to give cage hexakis(alkylgermasesquioxane)s, (RGe)(6)O-9. These structures of cage (RGe)(6)O-9 were fully confirmed by spectroscopic and X-ray diffraction methods. t-Butyldichloro(ethoxy)germane, t-BuGe(OEt)Cl-2, was carefully treated with water at 5 degreesC for 3 h to afford cis, trans-1,3,5-tri-t-butyl-1,3,5-trichlorocyclotrigermoxane, (t-BuClGeO)(3). Hydrolysis of (t-BuClGeO)(3) at 5 degreesC for additional 33 h gave a tricyclic anti-form ladder 5,7-dichloro-1,3,5,7,9,1 1-hexat-butyltricyclo[7.3.1.1(3.7)]hexagermoxanes, (t-BuGe)(6)O8Cl2. The tricyclic ladder (t-BuGe)(6)O8Cl2 was also prepared by hydrolysis of t-butyl(chloro)diethoxygermane, t-BuGe(OEt)(2)Cl, at 5 degreesC for 6 It, and its structure was determined by spectroscopic and X-ray diffraction analysis. The tricyclic ladder germoxane reacted with aqueous NaOH in xylene at 130-140 degreesC for 3 h to afford hexakis(t-butylgermasesquioxane), (t-BuGe)(6)O-9. The formation mechanism of the germasesquioxane, (t-BuGe)(6)O-9 from t-butyl(chloro)ethoxygermanes, t-BuGe(OEt)(n)Cl3-n (n = 0-3) is also discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
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