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1,4-Dimethoxy-2,5-bis[4-(trifluoromethyl)phenyl]benzene | 896732-25-5

中文名称
——
中文别名
——
英文名称
1,4-Dimethoxy-2,5-bis[4-(trifluoromethyl)phenyl]benzene
英文别名
——
1,4-Dimethoxy-2,5-bis[4-(trifluoromethyl)phenyl]benzene化学式
CAS
896732-25-5
化学式
C22H16F6O2
mdl
——
分子量
426.358
InChiKey
JJZJPVUSUAJXJV-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):
    6.9
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    1,4-Dimethoxy-2,5-bis[4-(trifluoromethyl)phenyl]benzene 在 ammonium cerium (IV) nitrate 作用下, 以 乙腈 为溶剂, 以65%的产率得到2,5-bis-(4-trifluoromethylphenyl)-1,4-benzoquinone
    参考文献:
    名称:
    Controlling Site Selectivity in Pd-Catalyzed Oxidative Cross-Coupling Reactions
    摘要:
    This paper presents a detailed investigation of the factors controlling site selectivity in the Pd-mediated oxidative coupling of 1,3-disubstituted and 1,2,3-trisubstituted arenes (aryl -H) with cyclometalating substrates (L similar to C-H). The influence of both the concentration and the steric/electronic properties of the quinone promoter are studied in detail. In addition, the effect of steric/electronic modulation of the carboxylate ligand is discussed. Finally, we demonstrate that substitution of the carboxylate for a carbonate X-type ligand leads to a complete reversal in site selectivity for many arene substrates. The origins of these trends in site selectivity are discussed in the context of the mechanism of Pd-catalyzed oxidative cross-coupling.
    DOI:
    10.1021/ja1097918
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文献信息

  • Terphenyl dihydroxy monomers containing fluorine and fluorinated poly(arylene ether sulfide)s
    申请人:Lee Jae-Suk
    公开号:US20060183878A1
    公开(公告)日:2006-08-17
    The present invention relates to terphenyl dihydroxy monomers containing fluorine and fluorinated poly(arylene ether sulfide)s prepared by using the monomers, more particularly, terphenyl dihydroxy monomers containing both two hydroxy functional groups and fluorine and fluorinated poly(arylene ether sulfide)s prepared by an aromatic nucleophilic substitution polymerization (S N Ar) using the monomers, which are thus useful as optical materials in the field of information telecommunications.
  • TERPHENYL DIHYDROXY MONOMERS CONTAINING FLUORINE AND FLUORINATED POLY(ARYLENE ETHER SULFIDE)S
    申请人:LEE Jae-Suk
    公开号:US20090259017A1
    公开(公告)日:2009-10-15
    The present invention relates to terphenyl dihydroxy monomers containing fluorine and fluorinated poly(arylene ether sulfide)s prepared by using the monomers, more particularly, terphenyl dihydroxy monomers containing both two hydroxy functional groups and fluorine and fluorinated poly(arylene ether sulfide)s prepared by an aromatic nucleophilic substitution polymerization (S N Ar) using the monomers, which are thus useful as optical materials in the field of information telecommunications.
  • US7732560B2
    申请人:——
    公开号:US7732560B2
    公开(公告)日:2010-06-08
  • Controlling Site Selectivity in Pd-Catalyzed Oxidative Cross-Coupling Reactions
    作者:Thomas W. Lyons、Kami L. Hull、Melanie S. Sanford
    DOI:10.1021/ja1097918
    日期:2011.3.30
    This paper presents a detailed investigation of the factors controlling site selectivity in the Pd-mediated oxidative coupling of 1,3-disubstituted and 1,2,3-trisubstituted arenes (aryl -H) with cyclometalating substrates (L similar to C-H). The influence of both the concentration and the steric/electronic properties of the quinone promoter are studied in detail. In addition, the effect of steric/electronic modulation of the carboxylate ligand is discussed. Finally, we demonstrate that substitution of the carboxylate for a carbonate X-type ligand leads to a complete reversal in site selectivity for many arene substrates. The origins of these trends in site selectivity are discussed in the context of the mechanism of Pd-catalyzed oxidative cross-coupling.
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