2,4,6-trimethoxy-4'-(trifluoromethyl)biphenyl | 1262967-16-7

• 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: 2,4,6-trimethoxy-4'-(trifluoromethyl)biphenyl
• 英文别名: 1,3,5-Trimethoxy-2-[4-(trifluoromethyl)phenyl]benzene；1,3,5-trimethoxy-2-[4-(trifluoromethyl)phenyl]benzene
• CAS: 1262967-16-7
• 化学式: C₁₆H₁₅F₃O₃
• 分子量: 312.289
• InChiKey: SGDYNBDSAYFABK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  27.7
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  2,4,6-三甲氧基苯甲酸 、 三乙氧基[4-(三氟甲基)苯基]硅烷 在 palladium(II) trifluoroacetate 、 N-benzyl-N-[2-(dibenzylhydrazinylidene)ethylideneamino]-1-phenylmethanamine 、 silver fluoride 作用下， 以 N,N-二甲基乙酰胺 为溶剂， 反应 4.0h， 以48%的产率得到2,4,6-trimethoxy-4'-(trifluoromethyl)biphenyl
  参考文献：
  名称：

  Palladium-catalyzed decarboxylative coupling of benzoic acid derivatives using hydrazone ligands

  摘要：

  Palladium-catalyzed decarboxylative coupling of benzoic acid derivatives with arylboroxins gave biaryls using a catalytic amount of Pd(TFA)(2)-hydrazone Id system with Ag2CO3 at 80 degrees C in good yields. We also found that decarboxylative coupling with aryl(trialkoxy)silanes gave biaryls using a Pd(TFA)(2)-hydrazone 1g system with AgF in good yields. 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2014.04.017

文献信息

• Pd-catalysed decarboxylative Suzuki reactions and orthogonal Cu-based O-arylation of aromatic carboxylic acids
  作者：Jian-Jun Dai、Jing-Hui Liu、Dong-Fen Luo、Lei Liu

  DOI：10.1039/c0cc04104a

  日期：——

  Pd-catalysed decarboxylative Suzuki reactions and orthogonal Cu-based O-arylation reactions of aromatic carboxylic acids are reported. The new reactions may provide alternative routes for the synthesis of some biaryls and aromatic carboxylic esters.

  钯催化的脱羧Suzuki反应和芳香族羧酸的正交Cu基O-芳基化反应已有报道。新的反应可能为某些联芳基和芳族羧酸酯的合成提供替代途径。
• Synthesis of NHC Ligands Containing a Sulfoxide Moiety and Their Use in Cross-Coupling via a Au(I)/(III) Catalytic Cycle
  作者：Takanori Shibata、Rikako Nagai、Sari Okazaki、Shun Nishibe、Mamoru Ito

  DOI：10.1246/bcsj.20220013

  日期：2022.4.15

  We designed and synthesized a new series of NHCs with a sulfoxide moiety as a hemilabile ligand. We investigated the catalytic activities of Au(I)-NHC complexes in the strong oxidant-free cross-coupling of iodoarenes with 1,3,5-trimethoxybenzene. We ascertained that the sulfoxide moiety is critical for the Au(I)/(III) catalytic cycle.

  我们设计并合成了一系列新的以亚砜部分作为半可配体的 NHC。我们研究了 Au(I)-NHC 配合物在碘芳烃与 1,3,5-三甲氧基苯的无强氧化剂交叉偶联中的催化活性。我们确定亚砜部分对 Au(I)/(III) 催化循环至关重要。