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1-chloro-3-((triethylsilyl)ethynyl)-2,5-dihydroxy-4-((methoxymethoxy)methyl)benzene | 1239333-74-4

中文名称
——
中文别名
——
英文名称
1-chloro-3-((triethylsilyl)ethynyl)-2,5-dihydroxy-4-((methoxymethoxy)methyl)benzene
英文别名
5-Chloro-2-(methoxymethoxymethyl)-3-(2-triethylsilylethynyl)benzene-1,4-diol
1-chloro-3-((triethylsilyl)ethynyl)-2,5-dihydroxy-4-((methoxymethoxy)methyl)benzene化学式
CAS
1239333-74-4
化学式
C17H25ClO4Si
mdl
——
分子量
356.922
InChiKey
WWZVXYWOTKXFCD-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):
    4.27
  • 重原子数:
    23
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    58.9
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-Chloro-2-(methoxymethoxymethyl)-3-(2-triethylsilylethynyl)cyclohexa-2,5-diene-1,4-dione高邻苯二甲酸酐lithium diisopropyl amide氯化铵 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 0.08h, 以52%的产率得到3-((triethylsilyl)ethynyl)-9-hydroxy-2-((methoxymethoxy)methyl)-1,4-anthraquinone
    参考文献:
    名称:
    Synthetic Studies on Lactonamycins: Synthesis of the Model BCDEF Aglycon
    摘要:
    The lactonamycin model aglycon 4 was synthesized from the trihalogenated benzene derivative 10. Ethynyltetraol 6 was prepared from 10 via carbon elongations, oxidative demethylation, a cycloaddition reaction with the diene derived from homophthalic anhydride, and dihydroxylation. Final E- and F-ring constructions from 6 were realized via a palladium-catalyzed cyclization-methoxycarbonylation, a stereoselective methanol addition, and lactonization, leading to the production of 4.
    DOI:
    10.1021/jo100913s
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文献信息

  • Synthetic Studies on Lactonamycins: Synthesis of the Model BCDEF Aglycon
    作者:Kana Watanabe、Yusuke Iwata、Satoshi Adachi、Tomoyuki Nishikawa、Yuko Yoshida、Shunsuke Kameda、Mitsuaki Ide、Yoko Saikawa、Masaya Nakata
    DOI:10.1021/jo100913s
    日期:2010.8.20
    The lactonamycin model aglycon 4 was synthesized from the trihalogenated benzene derivative 10. Ethynyltetraol 6 was prepared from 10 via carbon elongations, oxidative demethylation, a cycloaddition reaction with the diene derived from homophthalic anhydride, and dihydroxylation. Final E- and F-ring constructions from 6 were realized via a palladium-catalyzed cyclization-methoxycarbonylation, a stereoselective methanol addition, and lactonization, leading to the production of 4.
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