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methyl 3-(2-chloro-1-formylcyclohex-2-enyl)propanoate | 1260150-11-5

中文名称
——
中文别名
——
英文名称
methyl 3-(2-chloro-1-formylcyclohex-2-enyl)propanoate
英文别名
Methyl 3-(2-chloro-1-formylcyclohex-2-en-1-yl)propanoate;methyl 3-(2-chloro-1-formylcyclohex-2-en-1-yl)propanoate
methyl 3-(2-chloro-1-formylcyclohex-2-enyl)propanoate化学式
CAS
1260150-11-5
化学式
C11H15ClO3
mdl
——
分子量
230.691
InChiKey
AOJPKIPCEVDCTN-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):
    1.8
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    丙烯酸甲酯(MA)2-氯-1-甲酰基-1-环己烯四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 0.42h, 以52%的产率得到methyl 3-(2-chloro-1-formylcyclohex-2-enyl)propanoate
    参考文献:
    名称:
    Cross-Coupling Reactions of Two Different Activated Alkenes through Tetrabutylammonium Fluoride (TBAF) Promoted Deprotonation/Activation Strategy: A Regioselective Construction of Quaternary Carbon Centers
    摘要:
    A novel TBAF-promoted intermolecular crossed-conjugate addition has been developed. For a range of cyclic beta-halo-alpha,beta-unsaturated carbonyl compounds, the vinylogous enolates generated by deprotonation at the gamma-position preferentially reacted with Michael acceptors at the alpha-position to deliver cross-coupling products in good yields.
    DOI:
    10.1021/ol1028332
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文献信息

  • Cross-Coupling Reactions of Two Different Activated Alkenes through Tetrabutylammonium Fluoride (TBAF) Promoted Deprotonation/Activation Strategy: A Regioselective Construction of Quaternary Carbon Centers
    作者:Jing-Li Zhang、Yue-Fa Gong
    DOI:10.1021/ol1028332
    日期:2011.1.21
    A novel TBAF-promoted intermolecular crossed-conjugate addition has been developed. For a range of cyclic beta-halo-alpha,beta-unsaturated carbonyl compounds, the vinylogous enolates generated by deprotonation at the gamma-position preferentially reacted with Michael acceptors at the alpha-position to deliver cross-coupling products in good yields.
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