N-(2,4-dichlorophenyl)-2,6-difluorobenzamide | 406926-84-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(2,4-dichlorophenyl)-2,6-difluorobenzamide
• CAS: 406926-84-9
• 化学式: C₁₃H₇Cl₂F₂NO
• 分子量: 302.107
• InChiKey: FPLBPRYXNNIQDR-UHFFFAOYSA-N

物化性质

• 沸点：
  312.8±42.0 °C(Predicted)
• 密度：
  1.505±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.52
• 重原子数：
  19.0
• 可旋转键数：
  2.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  29.1
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  N-(2,4-dichlorophenyl)-2,6-difluorobenzamide 在 dipotassium peroxodisulfate 、 [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂ 、 三氟乙酸 、 三氟乙酸酐 作用下， 反应 16.0h， 以79%的产率得到N-(2,4-dichloro-6-hydroxyphenyl)-2,6-difluorobenzamide
  参考文献：
  名称：

  Synthesis of 2-Aminophenols and Heterocycles by Ru-Catalyzed C–H Mono- and Dihydroxylation

  摘要：

  A novel and efficient synthesis of 2-aminophenols, 2-aminobenzene-1,3-diols, and heterocycles through Ru-catalyzed C-H mono- and dihydroxylation of anilides has been developed with a new directing group strategy. The reaction demonstrates excellent reactivity, regioselectivity, good functional group tolerance, and high yields.

  DOI：

  10.1021/ol400437a
• 作为产物：
  描述：

  2,6-二氟苯甲酸 在 氯化亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 17.0h， 生成 N-(2,4-dichlorophenyl)-2,6-difluorobenzamide
  参考文献：
  名称：

  Synthesis of 2-Aminophenols and Heterocycles by Ru-Catalyzed C–H Mono- and Dihydroxylation

  摘要：

  A novel and efficient synthesis of 2-aminophenols, 2-aminobenzene-1,3-diols, and heterocycles through Ru-catalyzed C-H mono- and dihydroxylation of anilides has been developed with a new directing group strategy. The reaction demonstrates excellent reactivity, regioselectivity, good functional group tolerance, and high yields.

  DOI：

  10.1021/ol400437a

文献信息

• Mixing <i>O</i>-Containing and <i>N</i>-Containing Directing Groups for C–H Activation: A Strategy for the Synthesis of Highly Functionalized 2,2′-Biaryls
  作者：Chao Zhang、Yugang Song、Zhihui Sang、Lingpeng Zhan、Yu Rao

  DOI：10.1021/acs.joc.7b02863

  日期：2018.3.2

  N-containing directing groups has been developed for the synthesis of 2,2′-biaryl via Pd-mediated C–H bond activation and oxidative coupling. This new transformation may proceed through a mechanism involving Pd(II) and Pd(IV) intermediates. We found the use of PTSA and HFIP to be critical for the reaction and suggest that these reagents could serve as efficient ligands for this C–C bond formation. This

  已经开发了一种结合含O和N的导向基团的策略，以通过Pd介导的C–H键活化和氧化偶联合成2，2′-联芳基。这种新的转化可能会通过涉及Pd（II）和Pd（IV）中间体的机制进行。我们发现使用PTSA和HFIP对于反应至关重要，并建议这些试剂可以作为这种C–C键形成的有效配体。该方法提供了广泛的官能团耐受性，出色的反应性和高收率。
• Synthesis of 2-Aminophenols and Heterocycles by Ru-Catalyzed C–H Mono- and Dihydroxylation
  作者：Xinglin Yang、Gang Shan、Yu Rao

  DOI：10.1021/ol400437a

  日期：2013.5.17

  A novel and efficient synthesis of 2-aminophenols, 2-aminobenzene-1,3-diols, and heterocycles through Ru-catalyzed C-H mono- and dihydroxylation of anilides has been developed with a new directing group strategy. The reaction demonstrates excellent reactivity, regioselectivity, good functional group tolerance, and high yields.