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methyl 2-(5-hexynyl)-6-oxocyclohexanecarboxylate | 1092716-95-4

中文名称
——
中文别名
——
英文名称
methyl 2-(5-hexynyl)-6-oxocyclohexanecarboxylate
英文别名
——
methyl 2-(5-hexynyl)-6-oxocyclohexanecarboxylate化学式
CAS
1092716-95-4
化学式
C14H20O3
mdl
——
分子量
236.311
InChiKey
SNYOKEKCHYYIQE-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):
    2.34
  • 重原子数:
    17.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    methyl 2-(5-hexynyl)-6-oxocyclohexanecarboxylateindium(III) tris[bis(trifluoromethanesulfonyl)amide] 作用下, 以 甲苯 为溶剂, 反应 108.0h, 生成 methyl 2-methylene-11-oxobicyclo[5.4.0]undecanecarboxylate 、 methyl (1R*, 7R*)-2-methylene-11-oxobicyclo[5.4.0]undecanecarboxylate
    参考文献:
    名称:
    Efficient Formation of Ring Structures Utilizing Multisite Activation by Indium Catalysis
    摘要:
    Lewis acidic indium(III) salts, in particular In(NTf2)(3), effect the conversion of alpha-(omega'-alkynyl)-beta-ketoesters; and omega-alkynyl-beta-ketoesters to the corresponding cyclic products in a manner known as the Coniaene reaction. This reaction can lead to the creation of five- to fifteen-membered-ring carbocycles and heterocycles in good to excellent yields. The synthetic features of the reaction are a relatively low catalyst loading, as low as 0.01 mol % in the best case, as well as no requirement of solvent for five-membered-ring formation and the requirement of only moderately dilute reaction conditions for medium-sized-ring formation. The high reactivity of indium salts is due to the double activation of the beta-ketoester substrate containing an acetylene function. The indium metal activates the beta-ketoester moiety by the formation of an indium enolate, and this indium metal electrophilically activates the alkyne moiety. Such a strong push-pull activation of the substrate by a single metal circumvents the disadvantage of entropic and enthalpic factors generally associated with the formation of medium- and large-sized rings. The reaction allows the ready formation of a fifteen-membered-ring carbocycle, from which di-muscone has been synthesized.
    DOI:
    10.1021/ja805657h
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