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3,3'-dicyclopentyl-1,1'-bi(bicyclo[1.1.1]pentane)

中文名称
——
中文别名
——
英文名称
3,3'-dicyclopentyl-1,1'-bi(bicyclo[1.1.1]pentane)
英文别名
1-Cyclopentyl-3-(3-cyclopentyl-1-bicyclo[1.1.1]pentanyl)bicyclo[1.1.1]pentane
3,3'-dicyclopentyl-1,1'-bi(bicyclo[1.1.1]pentane)化学式
CAS
——
化学式
C20H30
mdl
——
分子量
270.458
InChiKey
RHRCPQXVEGBHAW-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):
    7.4
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    1.0
  • 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:
    [1.1.1]螺桨烷Cyclopentylmagnesium chloride双(乙腈)氯化钯(II) 作用下, 以 乙醚 为溶剂, 反应 96.0h, 以60%的产率得到3,3'-dicyclopentyl-1,1'-bi(bicyclo[1.1.1]pentane)
    参考文献:
    名称:
    A Facile, Palladium-Catalyzed Synthesis of 1,1′-Bi(bicyclo[1.1.1]pentanes)
    摘要:
    Symmetrically 3,3'-disubstituted 1,1'-bi(bicyclo[1.1.1]pentanes) were synthesized in a four-step procedure, using commercially available starting materials, in fair overall yields (51-60%). In this synthesis the final step is an unexpected bridgehead-to-bridgehead homocoupling of bicyclo[1.1.1]pent-1-ylmagnesium halide catalyzed by palladium(II). Only 1.1 mol percent of bis(acetonitrile)palladium(II) chloride and two equivalents of bromomethane were necessary to accomplish this reaction. The bromomethane is essential to convert Pd-0 into Pd-II. The X-ray structure of the [2]staffane 1c has been determined and shows a nonbonded C1-C3 distance of 1.907 Angstrom in the bicyclo[1.1.1]pentyl subunit.
    DOI:
    10.1002/1099-0690(200103)2001:6<1049::aid-ejoc1049>3.0.co;2-v
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文献信息

  • A Facile, Palladium-Catalyzed Synthesis of 1,1′-Bi(bicyclo[1.1.1]pentanes)
    作者:J. D. Daniel Rehm、Burkhard Ziemer、Günter Szeimies
    DOI:10.1002/1099-0690(200103)2001:6<1049::aid-ejoc1049>3.0.co;2-v
    日期:2001.3
    Symmetrically 3,3'-disubstituted 1,1'-bi(bicyclo[1.1.1]pentanes) were synthesized in a four-step procedure, using commercially available starting materials, in fair overall yields (51-60%). In this synthesis the final step is an unexpected bridgehead-to-bridgehead homocoupling of bicyclo[1.1.1]pent-1-ylmagnesium halide catalyzed by palladium(II). Only 1.1 mol percent of bis(acetonitrile)palladium(II) chloride and two equivalents of bromomethane were necessary to accomplish this reaction. The bromomethane is essential to convert Pd-0 into Pd-II. The X-ray structure of the [2]staffane 1c has been determined and shows a nonbonded C1-C3 distance of 1.907 Angstrom in the bicyclo[1.1.1]pentyl subunit.
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