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(1-methyl-5-ferrocenyl-1H-pyrazol-3-yl)methanol | 1309044-83-4

中文名称
——
中文别名
——
英文名称
(1-methyl-5-ferrocenyl-1H-pyrazol-3-yl)methanol
英文别名
——
(1-methyl-5-ferrocenyl-1H-pyrazol-3-yl)methanol化学式
CAS
1309044-83-4
化学式
C15H16FeN2O
mdl
——
分子量
296.152
InChiKey
PZWJJLLHIXKHIV-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

反应信息

  • 作为反应物:
    描述:
    (1-methyl-5-ferrocenyl-1H-pyrazol-3-yl)methanol 在 MnO2 作用下, 以 二氯甲烷 为溶剂, 以94%的产率得到5-ferrocenyl-1-methyl-1H-pyrazole-3-carbaldehyde
    参考文献:
    名称:
    Synthesis and properties of 5-ferrocenyl-1H-pyrazole-3-carbaldehydes
    摘要:
    New ferrocene derivatives - ethyl esters of 1-aryl-5-ferrocenyl-1H-pyrazole-3-carboxylic acids were synthesized. The corresponding aldehydes were obtained from acid esters in two steps. The reductive amination reaction of 5-ferrocenyl-1-phenyl-1H-pyrazole-3-carbaldehyde was studied. Several of these compounds were investigated by cyclic voltammetry. All of them exhibited a reversible one-electron oxidation-reduction wave owing to the ferrocene-ferricinium redox couple with a positive shift (0.51-0.69 V) compared with that of ferrocene (0.46 V). The X-ray crystal structure of the ethyl ether 1-(3-chloro-2-fluorophenyl)-5-ferrocenyl-1H-pyrazole-3-carboxylic acid is also presented. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2010.11.018
  • 作为产物:
    描述:
    lithium aluminium tetrahydride 、 ethyl 5-ferrocenyl-1-methyl-1H-pyrazole-3-carboxylate hemihydrate 以 四氢呋喃1,4-二氧六环 为溶剂, 以96%的产率得到(1-methyl-5-ferrocenyl-1H-pyrazol-3-yl)methanol
    参考文献:
    名称:
    Synthesis and properties of 5-ferrocenyl-1H-pyrazole-3-carbaldehydes
    摘要:
    New ferrocene derivatives - ethyl esters of 1-aryl-5-ferrocenyl-1H-pyrazole-3-carboxylic acids were synthesized. The corresponding aldehydes were obtained from acid esters in two steps. The reductive amination reaction of 5-ferrocenyl-1-phenyl-1H-pyrazole-3-carbaldehyde was studied. Several of these compounds were investigated by cyclic voltammetry. All of them exhibited a reversible one-electron oxidation-reduction wave owing to the ferrocene-ferricinium redox couple with a positive shift (0.51-0.69 V) compared with that of ferrocene (0.46 V). The X-ray crystal structure of the ethyl ether 1-(3-chloro-2-fluorophenyl)-5-ferrocenyl-1H-pyrazole-3-carboxylic acid is also presented. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2010.11.018
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