2,6-二甲氧基-4'-氟联苯 | 1019777-19-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2,6-二甲氧基-4'-氟联苯
• 英文名称: 2,6-dimethoxy-4'-fluorobiphenyl
• 英文别名: 4'-fluoro-2,6-dimethoxybiphenyl；2-(4-Fluorophenyl)-1,3-dimethoxybenzene；2-(4-fluorophenyl)-1,3-dimethoxybenzene
• CAS: 1019777-19-5
• 化学式: C₁₄H₁₃FO₂
• 分子量: 232.254
• InChiKey: SVDXLPFVQKOTFX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2,6-二甲氧基苯硼酸 、 对溴氟苯 在 dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) 、 三乙胺 作用下， 以 水 为溶剂， 反应 24.0h， 以99%的产率得到2,6-二甲氧基-4'-氟联苯
  参考文献：
  名称：

  Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles

  摘要：

  Use of a dilute aqueous solution containing a nonionic amphiphile allows efficient Suzuki-Miyaura cross-couplings of arylboronic acids with a wide array of aryl halides and pseudohalides, including sterically hindered and lipophilic substrates, in most cases at room temperature.

  DOI：

  10.1021/ol702714y

文献信息

• Biaryl Synthesis via Decarboxylative Pd-Catalyzed Reactions of Arenecarboxylic Acids and Diaryliodonium Triflates
  作者：Jean-Michel Becht、Claude Le Drian

  DOI：10.1021/ol8011293

  日期：2008.7.17

  A novel simple and efficient synthesis of biaryls via a Pd-catalyzed decarboxylative cross-coupling reaction of arenecarboxylic acids and diaryliodonium triflates is described. The PdCl2/DPEphos catalytic system in the presence of Ag2CO3 in DMSO was found to be the most efficient. Various biaryls, including sterically hindered biaryls, were synthesized with yields ranging from 37 to 85%.

  描述了通过芳烃羧酸和二芳基don鎓三氟甲磺酸酯的Pd催化的脱羧交叉偶联反应的新颖简单有效的联芳基合成。发现在DMSO中存在Ag2CO3的情况下，PdCl2 / DPEphos催化体系最为有效。合成了包括空间位阻联芳基在内的各种联芳基，收率范围为37％至85％。
• Palladium-Catalyzed Stille Cross-Coupling Reaction of Aryl Chlorides using a Pre-Milled Palladium Acetate and XPhos Catalyst System
  作者：John R. Naber、Stephen L. Buchwald

  DOI：10.1002/adsc.200800032

  日期：2008.5.5

  highly active catalyst system based upon a biaryl monophosphine ligand, XPhos, for the palladium-catalyzed Stille reaction has been developed. This method allows for the coupling of aryl chlorides with a range of tributylarylstannanes to produce the corresponding biaryl compounds in good to excellent yields (61–98%) in short reaction times (4 h). Palladium(II) acetate [Pd(OAc)2] and XPhos in a 1:1.1 ratio

  已经开发出了基于联芳基单膦配体XPhos的高活性催化剂体系，用于钯催化的Stille反应。这种方法可以使芳基氯化物与一系列的三丁基芳基锡烷偶联，从而在较短的反应时间（4小时）内以良好或优异的收率（61-98％）生产相应的联芳基化合物。将醋酸钯（II）[Pd（OAc）2 ]和XPhos以1：1.1的比例研磨成细粉，用作这些反应的预催化剂。
• Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles
  作者：Bruce H. Lipshutz、Tue B. Petersen、Alexander R. Abela

  DOI：10.1021/ol702714y

  日期：2008.4.1

  Use of a dilute aqueous solution containing a nonionic amphiphile allows efficient Suzuki-Miyaura cross-couplings of arylboronic acids with a wide array of aryl halides and pseudohalides, including sterically hindered and lipophilic substrates, in most cases at room temperature.