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methyl 2-oxo-15-methylcyclopentadecane-1-carboxylate | 1000014-61-8

中文名称
——
中文别名
——
英文名称
methyl 2-oxo-15-methylcyclopentadecane-1-carboxylate
英文别名
Methyl 2-methyl-15-oxocyclopentadecane-1-carboxylate
methyl 2-oxo-15-methylcyclopentadecane-1-carboxylate化学式
CAS
1000014-61-8
化学式
C18H32O3
mdl
——
分子量
296.45
InChiKey
MQEMLBWLSFGHAU-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):
    6.4
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    methyl 2-oxo-15-methylcyclopentadecane-1-carboxylate 在 sodium chloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 36.0h, 以7 mg的产率得到(±)-麝香酮
    参考文献:
    名称:
    铟催化的ω-炔基-β-酮酸酯的环异构化为6至15元环。
    摘要:
    DOI:
    10.1002/anie.200702928
  • 作为产物:
    描述:
    methyl 2-methyl-15-oxocyclopentadecene-1-carboxylate 在 palladium on activated charcoal 、 氢气 作用下, 以 乙醇 为溶剂, 反应 3.5h, 生成 methyl 2-oxo-15-methylcyclopentadecane-1-carboxylate
    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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