摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-trimethylsiloxy-3,7,10-trimethylgermatrane | 131498-79-8

中文名称
——
中文别名
——
英文名称
1-trimethylsiloxy-3,7,10-trimethylgermatrane
英文别名
——
1-trimethylsiloxy-3,7,10-trimethylgermatrane化学式
CAS
131498-79-8
化学式
C12H27GeNO4Si
mdl
——
分子量
350.026
InChiKey
DDPBADAKVHOYBX-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    1-trimethylsiloxy-3,7,10-trimethylgermatrane氢氟酸 作用下, 以 异丙醇 为溶剂, 以60%的产率得到1-fluoro-3,7,10-trimethylgermatrane
    参考文献:
    名称:
    A facile synthesis of 1-halo- and 1-organoxygermatranes
    摘要:
    Interaction of the readily available 1-trimethylsiloxygermatranes (1a, 1b) with various halogenating reagents (Me3SiBr, Me3SiI, HF and SOCl2) has given the 1-halogermatranes (2a-2f). The 1-halogermatranes (2a, 2b) have been converted into the corresponding 1-organoxygermatranes by treatment with trialkylalkoxystannanes (3a-3f). The corresponding 1-organoxygermatranes (4d, 4e, 4f) were made by interaction of 1-hydroxygermatrane monohydrate with the corresponding hydroxy derivatives).
    DOI:
    10.1016/0022-328x(91)83089-m
点击查看最新优质反应信息

文献信息

  • Preparation of germatranyl triflates: reactions of germatranes N(CH2CHRO)3X (X=Br, OTf, OSiMe3; R=H, Me) with lithium reagents
    作者:Sergey S. Karlov、Pavel L. Shutov、Novruz G. Akhmedov、Markus A. Seip、Jörg Lorberth*、Galina S. Zaitseva*
    DOI:10.1016/s0022-328x(99)00739-1
    日期:2000.4
    New germatranes N(CH2CHRO)(3)GeOTf (4a, R = H; 4b, R = Me) were prepared in quantitative yield by treatment of N(CH2CHRO)(3)GeOSiMe3 (2a and 2b), with Me3SiOTf. The reactions of germatranes N(CH2CHRO)(3)GeX [3a, X = Br, R = H; 4a, X = OSO2CF3, R = H; 4b, X = OSO2CF3, R = Me; 2a, X = OSiMe3, R = H; 2b, X = OSiMe3, R = Me] with LiY reagents were studied. A series of germatranes N(CH2CHRO)(3)GeY [5a, R = H, Y = Ind (indenyl); 5b, R = Me, Y = Ind; 6a, R = H, Y = N(SiMe3)(2); 6b, R = Me, Y = N(SiMe3)(2); 7a, R = H, Y = Cp (cyclopentadienyl); 7b, R = Me, Y = Cp; 8a, R = H, Y = Flu (fluorenyl); 9a, R = H, Y = t-Bu] were obtained by nucleophilic substitution with the corresponding LiY reagent. Reactions of N(CH2CHMeO)(3)GeOSiMe3 (2b) and N(CH2CH2O)(3)GeBr (3a) with excess n-BuLi and of N(CH2CH2O)(3)GeOSiMe3 (2a) with excess LiNMe2 led to the formation of n-Bu4Ge and (Me2N)(4)Ge, The structures of new germatranes 4a, 4b, 6b and 7b were confirmed by NMR spectroscopy, mass spectrometry and elemental analyses. (C) 2000 Elsevier Science S.A. All rights reserved.
查看更多