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2,2-dichloro-1,1-diferrocenylcyclopropane | 500213-77-4

中文名称
——
中文别名
——
英文名称
2,2-dichloro-1,1-diferrocenylcyclopropane
英文别名
cyclopenta-1,3-diene;5-(2,2-dichloro-1-cyclopenta-2,4-dien-1-ylcyclopropyl)cyclopenta-1,3-diene;iron(2+)
2,2-dichloro-1,1-diferrocenylcyclopropane化学式
CAS
500213-77-4
化学式
C23H20Cl2Fe2
mdl
——
分子量
479.012
InChiKey
PSBNKUXGBWYDMM-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:
    2,2-dichloro-1,1-diferrocenylcyclopropane 在 C2H5MgCl 、 Ti(OCH(CH3)2)4 作用下, 以 四氢呋喃乙醚 为溶剂, 以13%的产率得到1,1-diferrocenylcyclopropane
    参考文献:
    名称:
    摘要:
    2-Chloro-and 2-bromo-1,1-diferrocenylcyclopropanes were synthesized as Z- and E-isomers with respect to the ferrocenyl substituent having a bisector orientation. The structure of Z-2-chloro- 1, 1 -diferrocenylcyclopropane was confirmed by X-ray diffraction analysis. Treatment of the resulting monohalides with potassium tert-butoxide in dimethyl sulfoxide afforded 3,3-diferrocenylcyclopropene in 20%' yield. The small ring in halogen- substituted diferrocenylcyclopropanes and diferrocenylcyclopropene is readily cleaved to give predominantly 3-ferrocenyl-1H-cyclopentaferrocene.
    DOI:
    10.1023/a:1022460701988
  • 作为产物:
    描述:
    1,1-diferrocenylethylene苄基三乙基氯化铵 在 NaOH 作用下, 以 二氯甲烷氯仿 为溶剂, 以67%的产率得到2,2-dichloro-1,1-diferrocenylcyclopropane
    参考文献:
    名称:
    摘要:
    2-Chloro-and 2-bromo-1,1-diferrocenylcyclopropanes were synthesized as Z- and E-isomers with respect to the ferrocenyl substituent having a bisector orientation. The structure of Z-2-chloro- 1, 1 -diferrocenylcyclopropane was confirmed by X-ray diffraction analysis. Treatment of the resulting monohalides with potassium tert-butoxide in dimethyl sulfoxide afforded 3,3-diferrocenylcyclopropene in 20%' yield. The small ring in halogen- substituted diferrocenylcyclopropanes and diferrocenylcyclopropene is readily cleaved to give predominantly 3-ferrocenyl-1H-cyclopentaferrocene.
    DOI:
    10.1023/a:1022460701988
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文献信息

  • 3,3-Diferrocenylcyclopropene
    作者:Elena I. Klimova、Marcos Martı́nez Garcı́a、Tatiana Klimova、José M.Mendez Stivalet、Simón Hernández Ortega、Lena Ruı́z Ramı́rez
    DOI:10.1016/s0022-328x(02)01702-3
    日期:2002.10
    Dehydrohalogenation of isomeric 2-chloro- and 2-bromo-1,1-diferrocenyleyclopropanes (Z- and E-isomers with respect to the 'bisecting' ferrocenyl substituent) under the action of Bu'OK in DMSO afforded 3,3-diferrocenylcyclopropene. In solution, this underwent facile opening of the small ring to give 3-ferrocenyl-1H-cyclopentaferrocene ( similar to 55%) and 1,1-diferrocenylpropene (15%). The spatial structure of Z-2-chloro-1,1-diferrocenylcyclopropane and 1,1-diferrocenylcyclopropane were elucidated by X-ray diffraction analysis of a single crystal. (C) 2002 Elsevier Science B.V. All rights reserved.
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