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1-(3-hydroxypent-1-en-4-ynyl)-6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-triene

中文名称
——
中文别名
——
英文名称
1-(3-hydroxypent-1-en-4-ynyl)-6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-triene
英文别名
(E)-1-[6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-trien-1-yl]pent-1-en-4-yn-3-ol
1-(3-hydroxypent-1-en-4-ynyl)-6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-triene化学式
CAS
——
化学式
C15H14O2
mdl
——
分子量
226.275
InChiKey
AEJWMFXPJDQGQA-MDZDMXLPSA-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):
    1.3
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-(3-hydroxypent-1-en-4-ynyl)-6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-trienebarium permanganate 作用下, 以 二氯甲烷 为溶剂, 反应 3.5h, 以84%的产率得到1-(3-oxopent-1-en-4-ynyl)-6-(oxoprop-2-ynyl)cyclohepta-1,3,5-triene
    参考文献:
    名称:
    Syntheses and properties of methano-bridged dichlorodidehydro-[16]-, -[20]-and-[24]-annulenediones
    摘要:
    Bisethynylation of the vinylogous dialdehydes of cyclohepta-1.3,5-triene-1,6-dicarbaldehyde with ethynylmagnesium bromide followed by oxidation of the resulted diols afforded the diacetylenic diketones. Intramolecular oxidative coupling of these diketones under the Glaser conditions unexpectedly afforded three annulenediones with a 1,4-dichlorobutatriene moiety. The unusual structures were confirmed by X-ray crystallographic analysis of 10,13-dichloro-11.12-didehydro-1,6methano[16]annulene-9,1 4-dione. These annulenediones exhibited strong diatropicity in D2SO4 due to the dicationic 14 pi-, 18 pi- and 22 pi-electron species and their diatropicities were shown to increase with increasing ring size.
    DOI:
    10.1039/p19940001453
  • 作为产物:
    描述:
    1-formyl-6-(2-formylvinyl)cyclohepta-1,3,5-triene乙炔基溴化镁四氢呋喃 为溶剂, 反应 1.5h, 以53%的产率得到1-(3-hydroxypent-1-en-4-ynyl)-6-(1-hydroxyprop-2-ynyl)cyclohepta-1,3,5-triene
    参考文献:
    名称:
    Syntheses and properties of methano-bridged dichlorodidehydro-[16]-, -[20]-and-[24]-annulenediones
    摘要:
    Bisethynylation of the vinylogous dialdehydes of cyclohepta-1.3,5-triene-1,6-dicarbaldehyde with ethynylmagnesium bromide followed by oxidation of the resulted diols afforded the diacetylenic diketones. Intramolecular oxidative coupling of these diketones under the Glaser conditions unexpectedly afforded three annulenediones with a 1,4-dichlorobutatriene moiety. The unusual structures were confirmed by X-ray crystallographic analysis of 10,13-dichloro-11.12-didehydro-1,6methano[16]annulene-9,1 4-dione. These annulenediones exhibited strong diatropicity in D2SO4 due to the dicationic 14 pi-, 18 pi- and 22 pi-electron species and their diatropicities were shown to increase with increasing ring size.
    DOI:
    10.1039/p19940001453
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文献信息

  • Higuchi Hiroyuki, Asano Kaori, Ojima Juro, Yamamoto Koji, Yoshida Toshika+, J. Chem. Soc. Perkin Trans. 1, (1994) N 11, S 1453-1468
    作者:Higuchi Hiroyuki, Asano Kaori, Ojima Juro, Yamamoto Koji, Yoshida Toshika+
    DOI:——
    日期:——
  • Syntheses and properties of methano-bridged dichlorodidehydro-[16]-, -[20]-and-[24]-annulenediones
    作者:Hiroyuki Higuchi、Kaori Asano、J?ro Ojima、Koji Yamamoto、Toshikatsu Yoshida、Tomohiro Adachi、Gaku Yamamoto
    DOI:10.1039/p19940001453
    日期:——
    Bisethynylation of the vinylogous dialdehydes of cyclohepta-1.3,5-triene-1,6-dicarbaldehyde with ethynylmagnesium bromide followed by oxidation of the resulted diols afforded the diacetylenic diketones. Intramolecular oxidative coupling of these diketones under the Glaser conditions unexpectedly afforded three annulenediones with a 1,4-dichlorobutatriene moiety. The unusual structures were confirmed by X-ray crystallographic analysis of 10,13-dichloro-11.12-didehydro-1,6methano[16]annulene-9,1 4-dione. These annulenediones exhibited strong diatropicity in D2SO4 due to the dicationic 14 pi-, 18 pi- and 22 pi-electron species and their diatropicities were shown to increase with increasing ring size.
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