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dicarbonyl(methoxycarbonylvinylidene)bis(triethylphosphane)iron | 198569-50-5

中文名称
——
中文别名
——
英文名称
dicarbonyl(methoxycarbonylvinylidene)bis(triethylphosphane)iron
英文别名
——
CAS
198569-50-5
化学式
C18H34FeO4P2
mdl
——
分子量
432.26
InChiKey
ITAXSFVBYOEKNA-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:
    dicarbonyl(methoxycarbonylvinylidene)bis(triethylphosphane)iron丙炔酸甲酯乙醚 为溶剂, 以9%的产率得到carbonyl[2,4,6-tris(methoxycarbonyl)-hexa-1,3,5-trien-1,5-diyl]bis(triethylphosphane)iron
    参考文献:
    名称:
    Methyl propiolate coupling at the Fe(CO)2(PEt3)2 fragment
    摘要:
    The in situ solution mixture of Fe(CO)(2)(PEt3)(2)(N-2) 3a and (mu-N-2)[Fe(CO)(2)(PEt3)(2)](2) 3b reacts with HC=CCOOMe to afford an acetylene Fe(CO)(2)(PEt3)(2)(eta(2)-HC=CCOOMe) 4a and an acetylido hydride complex Fe(CO)(2)(PEt3)(2)(H)(C=CCOOMe) 4b as primary products. Compounds 4a and 4b are in equilibrium. The equilibrium mixture is irreversibly converted to a vinylidene species Fe(CO)(2)(PEt3)(2)(C=CHCOOMe) 5 in the presence of silylated silica. Addition of further equivalents of HC=CCOOMe to 5 leads to the isolation of carbonyl[2,4,6-tris(methyoxycarbonyl)-hexa-1,3,5-trien-1,5-diyl]bis(triethylphosphane)iron 9 and dicarbonyl[methoxycarbonyl(1,4-di-methoxycarbonyl-buta-1,3-dien-2-y)vinylidene]bis(triethylphosphane)iron 10 as iron-bound trimerization products of HC=CCOOMe. 10 was characterized by a single crystal X-ray diffraction study. (C) 1997 Elsevier Science S.A.
    DOI:
    10.1016/s0022-328x(97)00132-0
  • 作为产物:
    描述:
    dicarbonyl(methylpropyonate)bis(triethylphosphane)iron 、 dicarbonylhydrido(methylpropyonate-1-yl)bis(triethylphosphane)iron 在 SiO2 作用下, 以 正己烷 为溶剂, 以58%的产率得到dicarbonyl(methoxycarbonylvinylidene)bis(triethylphosphane)iron
    参考文献:
    名称:
    Methyl propiolate coupling at the Fe(CO)2(PEt3)2 fragment
    摘要:
    The in situ solution mixture of Fe(CO)(2)(PEt3)(2)(N-2) 3a and (mu-N-2)[Fe(CO)(2)(PEt3)(2)](2) 3b reacts with HC=CCOOMe to afford an acetylene Fe(CO)(2)(PEt3)(2)(eta(2)-HC=CCOOMe) 4a and an acetylido hydride complex Fe(CO)(2)(PEt3)(2)(H)(C=CCOOMe) 4b as primary products. Compounds 4a and 4b are in equilibrium. The equilibrium mixture is irreversibly converted to a vinylidene species Fe(CO)(2)(PEt3)(2)(C=CHCOOMe) 5 in the presence of silylated silica. Addition of further equivalents of HC=CCOOMe to 5 leads to the isolation of carbonyl[2,4,6-tris(methyoxycarbonyl)-hexa-1,3,5-trien-1,5-diyl]bis(triethylphosphane)iron 9 and dicarbonyl[methoxycarbonyl(1,4-di-methoxycarbonyl-buta-1,3-dien-2-y)vinylidene]bis(triethylphosphane)iron 10 as iron-bound trimerization products of HC=CCOOMe. 10 was characterized by a single crystal X-ray diffraction study. (C) 1997 Elsevier Science S.A.
    DOI:
    10.1016/s0022-328x(97)00132-0
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