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1,2,4,5-tetrakis(E)-[2-(4-pentyloxyphenyl)vinyl]benzene | 1416403-60-5

中文名称
——
中文别名
——
英文名称
1,2,4,5-tetrakis(E)-[2-(4-pentyloxyphenyl)vinyl]benzene
英文别名
1,2,4,5-tetrakis[(E)-2-(4-pentoxyphenyl)ethenyl]benzene
1,2,4,5-tetrakis(E)-[2-(4-pentyloxyphenyl)vinyl]benzene化学式
CAS
1416403-60-5
化学式
C58H70O4
mdl
——
分子量
831.191
InChiKey
IPLJICITCDHVJU-BIDHLLRRSA-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):
    18.1
  • 重原子数:
    62
  • 可旋转键数:
    28
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1,2,4,5-四溴苯1-溴戊烷甲基三苯基碘化膦对羟基苯甲醛1,3-bis[(diphenylphosphino)propane]dichloronickel(II)四丁基溴化铵 、 palladium diacetate 、 potassium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 40.0h, 以17%的产率得到1,2,4,5-tetrakis(E)-[2-(4-pentyloxyphenyl)vinyl]benzene
    参考文献:
    名称:
    Synthesis of alkyloxy stilbenes by one-pot O-alkylation-Wittig and O-alkylation-Wittig–Heck reaction sequence
    摘要:
    A new route for the synthesis of allcyloxy stilbenes from hydroxy benzaldehydes is developed by a combination of one-pot reactions. Tandem one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reactions offer a simple access to conjugated alkyloxy stilbenes. A highly conjugated tetra(p-alkyloxystyryl) benzene was synthesized from 1,2,4,5-tetrabromobenzene involving a series of one-pot operations following the O-alkylation-Wittig-Heck scheme. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.10.102
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文献信息

  • Synthesis of alkyloxy stilbenes by one-pot O-alkylation-Wittig and O-alkylation-Wittig–Heck reaction sequence
    作者:Krupa N. Patel、Bola V. Kamath、Ashutosh V. Bedekar
    DOI:10.1016/j.tetlet.2012.10.102
    日期:2013.1
    A new route for the synthesis of allcyloxy stilbenes from hydroxy benzaldehydes is developed by a combination of one-pot reactions. Tandem one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reactions offer a simple access to conjugated alkyloxy stilbenes. A highly conjugated tetra(p-alkyloxystyryl) benzene was synthesized from 1,2,4,5-tetrabromobenzene involving a series of one-pot operations following the O-alkylation-Wittig-Heck scheme. (C) 2012 Elsevier Ltd. All rights reserved.
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