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2-diazonio-1,5-diethoxy-4-methoxy-5-oxopenta-1,3-dien-1-olate | 126554-43-6

中文名称
——
中文别名
——
英文名称
2-diazonio-1,5-diethoxy-4-methoxy-5-oxopenta-1,3-dien-1-olate
英文别名
——
2-diazonio-1,5-diethoxy-4-methoxy-5-oxopenta-1,3-dien-1-olate化学式
CAS
126554-43-6
化学式
C10H14N2O5
mdl
——
分子量
242.232
InChiKey
QREDZUMMTCHBPP-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):
    0.31
  • 重原子数:
    17.0
  • 可旋转键数:
    6.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    98.23
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    2-diazonio-1,5-diethoxy-4-methoxy-5-oxopenta-1,3-dien-1-olate 在 dirhodium tetraacetate 作用下, 以 二氯甲烷 为溶剂, 生成 1-((Z)-2-Ethoxycarbonyl-2-methoxy-vinyl)-2-oxo-cyclopent-3-enecarboxylic acid ethyl ester
    参考文献:
    名称:
    Versatile synthesis of tropones by reaction of rhodium(II)-stabilized vinylcarbenoids with 1-methoxy-1-[(trimethylsilyl)oxy]buta-1,3-diene
    摘要:
    Rhodium(II)-catalyzed decomposition of vinyldiazomethanes in the presence of 1-methoxy-1-[(trimethylsilyl)oxy]buta-1,3-diene leads to [3 + 4] annulation products by a tandem cyclopropanation/Cope rearrangement sequence. The resulting cycloheptadienes are readily converted to cycloheptatrienones either by hydrolysis with mild acid followed by oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone or by treatment with dichloroethoxyoxovanadium. The efficiency of the general strategy was demonstrated through a short synthesis of nezukone.
    DOI:
    10.1021/jo00022a041
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文献信息

  • Versatile synthesis of tropones by reaction of rhodium(II)-stabilized vinylcarbenoids with 1-methoxy-1-[(trimethylsilyl)oxy]buta-1,3-diene
    作者:Huw M. L. Davies、T. Jeffrey Clark、Garland F. Kimmer
    DOI:10.1021/jo00022a041
    日期:1991.10
    Rhodium(II)-catalyzed decomposition of vinyldiazomethanes in the presence of 1-methoxy-1-[(trimethylsilyl)oxy]buta-1,3-diene leads to [3 + 4] annulation products by a tandem cyclopropanation/Cope rearrangement sequence. The resulting cycloheptadienes are readily converted to cycloheptatrienones either by hydrolysis with mild acid followed by oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone or by treatment with dichloroethoxyoxovanadium. The efficiency of the general strategy was demonstrated through a short synthesis of nezukone.
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