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1-ethoxy-8-oxo-8H-indeno[2,3-d]pyrrole | 1148119-34-9

中文名称
——
中文别名
——
英文名称
1-ethoxy-8-oxo-8H-indeno[2,3-d]pyrrole
英文别名
——
1-ethoxy-8-oxo-8H-indeno[2,3-d]pyrrole化学式
CAS
1148119-34-9
化学式
C13H11NO2
mdl
——
分子量
213.236
InChiKey
CBLUGHNNZJZQDO-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):
    2.15
  • 重原子数:
    16.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    31.23
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为产物:
    描述:
    1H-茚-1,2,3-三酮2-肟乙烯基磷酸二乙酯sodium ethanolate 作用下, 反应 12.0h, 以46%的产率得到diethyl (5-oxo-4,5-dihydroindeno[2,3-b][1,4]oxazin-3-yl)phosphonate
    参考文献:
    名称:
    An efficient method for the synthesis of spiro and fused N-heterocyclic phosphor esters. Reactions of triketoindan-2-oxime with α-phosphonyl carbanions
    摘要:
    Treatment of triketoindan-2-oxime with alpha-phosphonyl carbanions in sodium ethanolate solution at reflux temperature led to a number of the corresponding substituted spiroisooxazole-, fused 1,3-oxazole, and 1,4-oxazine phosphor esters in moderate to high yields. Mechanisms for the formation of five- and six-membered rings are provided. A comparison of Wittig-Horner and Wittig reagent counterparts in reactions with the oxime is discussed. The various biological properties of selected examples of the synthesized products were studied.
    DOI:
    10.1007/s00706-007-0806-z
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文献信息

  • An efficient method for the synthesis of spiro and fused N-heterocyclic phosphor esters. Reactions of triketoindan-2-oxime with α-phosphonyl carbanions
    作者:Wafaa M. Abdou、Ashraf A. Sediek、Maha D. Khidre
    DOI:10.1007/s00706-007-0806-z
    日期:2008.6
    Treatment of triketoindan-2-oxime with alpha-phosphonyl carbanions in sodium ethanolate solution at reflux temperature led to a number of the corresponding substituted spiroisooxazole-, fused 1,3-oxazole, and 1,4-oxazine phosphor esters in moderate to high yields. Mechanisms for the formation of five- and six-membered rings are provided. A comparison of Wittig-Horner and Wittig reagent counterparts in reactions with the oxime is discussed. The various biological properties of selected examples of the synthesized products were studied.
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