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1,1'-bis[3-(2-trimethylsilyletoxy)propyl]ferrocene | 949107-86-2

中文名称
——
中文别名
——
英文名称
1,1'-bis[3-(2-trimethylsilyletoxy)propyl]ferrocene
英文别名
——
1,1'-bis[3-(2-trimethylsilyletoxy)propyl]ferrocene化学式
CAS
949107-86-2
化学式
C26H46FeO2Si2
mdl
——
分子量
502.668
InChiKey
NIJXVPBLFASTAO-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:
    1,1'-bis[3-(2-trimethylsilyletoxy)propyl]ferrocene盐酸 、 lithium tetrafluoroborate 、 作用下, 以 正己烷乙腈 为溶剂, 以72%的产率得到1,1'-di(3-hydroxypropyl)ferrocene
    参考文献:
    名称:
    1,1′-Bis(3-hydroxypropyl)ferrocene: Preparation and substitution with polyfluoroalkyl groups
    摘要:
    SiMe3CH2CH2 was demonstrated as a robust and convenient OH protecting group in the preparation of 1,1'-bis(3-hydroxypropyl)ferrocene (1). The OH groups were used to introduce polyfluorinated alkyl chains by acylation of 1 with (C2F5CO)20 and alkylation with CF3(CF2)(6)CH2OH under Mitsunobu reaction conditions. This demonstrates a new method for introduction of an omega-hydroxyalkyl group to the Cp unit as a synthetic handle for modification of molecular properties. (c) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2007.05.005
  • 作为产物:
    描述:
    3-(2-trimethylsilyletoxy)propylcyclopentadiene 、 iron(II) chloride 在 sodium hydride 作用下, 以 二甲基亚砜 为溶剂, 以84%的产率得到1,1'-bis[3-(2-trimethylsilyletoxy)propyl]ferrocene
    参考文献:
    名称:
    1,1′-Bis(3-hydroxypropyl)ferrocene: Preparation and substitution with polyfluoroalkyl groups
    摘要:
    SiMe3CH2CH2 was demonstrated as a robust and convenient OH protecting group in the preparation of 1,1'-bis(3-hydroxypropyl)ferrocene (1). The OH groups were used to introduce polyfluorinated alkyl chains by acylation of 1 with (C2F5CO)20 and alkylation with CF3(CF2)(6)CH2OH under Mitsunobu reaction conditions. This demonstrates a new method for introduction of an omega-hydroxyalkyl group to the Cp unit as a synthetic handle for modification of molecular properties. (c) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2007.05.005
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