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(Z)-3-(2,2-diethoxyethylidene)isobenzofuran-1(3H)-one | 1188414-13-2

中文名称
——
中文别名
——
英文名称
(Z)-3-(2,2-diethoxyethylidene)isobenzofuran-1(3H)-one
英文别名
(3Z)-3-(2,2-diethoxyethylidene)-2-benzofuran-1-one
(Z)-3-(2,2-diethoxyethylidene)isobenzofuran-1(3H)-one化学式
CAS
1188414-13-2
化学式
C14H16O4
mdl
——
分子量
248.279
InChiKey
HTICSQNTPLYLEU-XFXZXTDPSA-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):
    2.2
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    丙醛二乙基乙缩醛2-碘苯甲酸copper(l) iodidepotassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以70%的产率得到(Z)-3-(2,2-diethoxyethylidene)isobenzofuran-1(3H)-one
    参考文献:
    名称:
    轻度无钯条件下铜催化制备γ-亚烷基丁烯内酯和异香豆素
    摘要:
    Abstractmagnified imageA general and efficient copper(I)‐catalyzed cross‐coupling and heterocyclization reaction of terminal alkynes and β‐iodo‐α,β‐unsaturated acid derivatives has been developed under very mild conditions. This method provides easy access from good to excellent yields of a variety of 5‐ylidenebutenolides and 3‐substituted isocoumarins with excellent regio‐ and stereoselectivity. This procedure does not require the use of any expensive supplementary additives, and is palladium‐free.
    DOI:
    10.1002/adsc.200800757
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文献信息

  • Copper-Catalyzed Preparation of γ-Alkylidenebutenolides and Isocoumarins under Mild Palladium-Free Conditions
    作者:Samuel Inack-Ngi、Raphaël Rahmani、Laurent Commeiras、Gaëlle Chouraqui、Jérôme Thibonnet、Alain Duchêne、Mohamed Abarbri、Jean-Luc Parrain
    DOI:10.1002/adsc.200800757
    日期:2009.3
    Abstractmagnified imageA general and efficient copper(I)‐catalyzed cross‐coupling and heterocyclization reaction of terminal alkynes and β‐iodo‐α,β‐unsaturated acid derivatives has been developed under very mild conditions. This method provides easy access from good to excellent yields of a variety of 5‐ylidenebutenolides and 3‐substituted isocoumarins with excellent regio‐ and stereoselectivity. This procedure does not require the use of any expensive supplementary additives, and is palladium‐free.
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