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4-Hydroxy-6-oxo-2-phenyl-cyclohex-4-ene-1,3-dicarboxylic acid diethyl ester | 144284-94-6

中文名称
——
中文别名
——
英文名称
4-Hydroxy-6-oxo-2-phenyl-cyclohex-4-ene-1,3-dicarboxylic acid diethyl ester
英文别名
Diethyl 4-hydroxy-6-oxo-2-phenylcyclohex-4-ene-1,3-dicarboxylate
4-Hydroxy-6-oxo-2-phenyl-cyclohex-4-ene-1,3-dicarboxylic acid diethyl ester化学式
CAS
144284-94-6
化学式
C18H20O6
mdl
——
分子量
332.353
InChiKey
KPQCMDPVYPVFLL-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):
    2.6
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    89.9
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    4-Hydroxy-6-oxo-2-phenyl-cyclohex-4-ene-1,3-dicarboxylic acid diethyl esterN-(4-二甲氨基苄亚基)苯胺乙醇 为溶剂, 生成 diethyl 5-[[3,5-bis(ethoxycarbonyl)-2,6-dioxo-4-phenylcyclohexyl]-[4-(dimethylamino)phenyl]methyl]-4,6-dioxo-2-phenylcyclohexane-1,3-dicarboxylate
    参考文献:
    名称:
    New aspects in the reaction of azomethines with cyclic CH-acidic compounds
    摘要:
    Treatment of substituted benzylidene anilines 1 a - f with cyclic CH-acidic compounds 2 a - m in ethanol at room temperature yields in additon/elimination reactions the corresponding arylidene derivatives 4 and the 2 : 1 adducts 5. The addition products 3, which are formed as intermediates, could not be isolated in any case. The donor/acceptor effect of the substituents on the benzylidene moiety influences to a significant extent the reactivity towards the azomethine carbon.
    DOI:
    10.1007/bf00816851
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文献信息

  • New aspects in the reaction of azomethines with cyclic CH-acidic compounds
    作者:Lothar Hennig、Mario Alva-Astudillo、Gerhard Mann、Thomas Kappe
    DOI:10.1007/bf00816851
    日期:——
    Treatment of substituted benzylidene anilines 1 a - f with cyclic CH-acidic compounds 2 a - m in ethanol at room temperature yields in additon/elimination reactions the corresponding arylidene derivatives 4 and the 2 : 1 adducts 5. The addition products 3, which are formed as intermediates, could not be isolated in any case. The donor/acceptor effect of the substituents on the benzylidene moiety influences to a significant extent the reactivity towards the azomethine carbon.
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