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1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene | 925900-76-1

中文名称
——
中文别名
——
英文名称
1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene
英文别名
1,5-Bis(hex-1-ynyl)-2,4-bis(prop-2-enoxy)benzene;1,5-bis(hex-1-ynyl)-2,4-bis(prop-2-enoxy)benzene
1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene化学式
CAS
925900-76-1
化学式
C24H30O2
mdl
——
分子量
350.501
InChiKey
ZWSXQLUSNBUGNA-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):
    7.7
  • 重原子数:
    26
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzeneRuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 作用下, 以 二氯甲烷 为溶剂, 反应 8.0h, 以76%的产率得到4,6-bis(1'-butylethenyl)-2,8-dihydrobenzo-[1,2-b:5,4-b']dipyran
    参考文献:
    名称:
    An efficient synthesis of fused tricycles with a benzene core via intramolecular double ring-closing enyne metathesis
    摘要:
    A double enyne metathesis reaction has been developed for the efficient synthesis of tricyclic products with a benzene core in good yields. By this protocol, bisannulated benzenes with different ring sizes may he simultaneously constructed from the corresponding precursors in just 'one shot'. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.11.016
  • 作为产物:
    描述:
    4,6-diiodoresorcinol 在 bis-triphenylphosphine-palladium(II) chloride 吡啶 、 lithium hydroxide 、 copper(l) iodidepotassium carbonate三乙胺 作用下, 以 四氢呋喃甲醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 29.83h, 生成 1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene
    参考文献:
    名称:
    An efficient synthesis of fused tricycles with a benzene core via intramolecular double ring-closing enyne metathesis
    摘要:
    A double enyne metathesis reaction has been developed for the efficient synthesis of tricyclic products with a benzene core in good yields. By this protocol, bisannulated benzenes with different ring sizes may he simultaneously constructed from the corresponding precursors in just 'one shot'. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.11.016
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文献信息

  • Palladium-Catalyzed Double Annulations To Construct Multisubstituted Benzodifurans
    作者:Zhiqiang Liang、Shengming Ma、Jihong Yu、Ruren Xu
    DOI:10.1021/jo7016263
    日期:2007.11.1
    Efficient synthetic routes to construct multisubstituted benzo[1,2-b:5,4-b‘]difurans and benzo[1,2-b:4,5-b‘]difurans from bis(allyloxy)bis(alkynyl)benzenes or bis(alkynyl)dihydroxybenzenes and allylic halides utilizing palladium-catalyzed double annulations is reported. By further applying a double ring-closing metathesis reaction, pentacyclic compounds were also prepared.
    有效的合成路线来构建多取代苯并[1,2- b:5,4- b “] difurans和苯并[1,2- b:4,5- b ”]由二difurans(烯丙氧基)双(炔基)苯或据报道,利用钯催化的双环双(炔基)二羟基苯和烯丙基卤化物。通过进一步进行双闭环复分解反应,还制备了五环化合物。
  • An efficient synthesis of fused tricycles with a benzene core via intramolecular double ring-closing enyne metathesis
    作者:Zhiqiang Liang、Shengming Ma、Jihong Yu、Ruren Xu
    DOI:10.1016/j.tet.2006.11.016
    日期:2007.1
    A double enyne metathesis reaction has been developed for the efficient synthesis of tricyclic products with a benzene core in good yields. By this protocol, bisannulated benzenes with different ring sizes may he simultaneously constructed from the corresponding precursors in just 'one shot'. (c) 2006 Elsevier Ltd. All rights reserved.
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