methyl 3-(2-nitro-4-(trifluoromethyl)phenyl)propanoate | 1493774-30-3

• 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: methyl 3-(2-nitro-4-(trifluoromethyl)phenyl)propanoate
• 英文别名: 2-nitro-4-(trifluoromethyl)-benzenepropanoic acid methyl ester；methyl 3-[2-nitro-4-(trifluoromethyl)phenyl]propanoate
• CAS: 1493774-30-3
• 化学式: C₁₁H₁₀F₃NO₄
• 分子量: 277.2
• InChiKey: ZTCIWQGHQQEXKH-UHFFFAOYSA-N

物化性质

• 沸点：
  296.6±35.0 °C(Predicted)
• 密度：
  1.358±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  19
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  methyl 3-(2-nitro-4-(trifluoromethyl)phenyl)propanoate 在 3,5-二乙酰基-1,4-二氢-2,6-二甲基吡啶 、 camphor-10-sulfonic acid 、 [bis(2,2′‐bipyridine)ruthenium(II)](chloride)₂ hexahydrate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 16.0h， 生成
  参考文献：
  名称：

  Reductive Cyclizations of Nitroarenes to Hydroxamic Acids by Visible Light Photoredox Catalysis

  摘要：

  We have developed a photocatalytic reduction of nitroarenes as an efficient, chemoselective route to biologically important N-phenyl hydroxamic acid scaffolds. Optimal conditions call for 2.5 mol% of a ruthenium photocatalyst, visible light irradiation, and a dihydropyridine terminal reductant. Because of the mild nature of the visible light activation, functional groups that might be sensitive to other non-photochemical reduction methods are easily tolerated.

  DOI：

  10.1055/s-0033-1338419
• 作为产物：
  描述：

  methyl 3-(2-nitro-4-(trifluoromethyl)phenyl)acrylate 在 Wilkinson's catalyst 、 氢气 作用下， 以 四氢呋喃 、 叔丁醇 为溶剂， 反应 48.0h， 以77%的产率得到methyl 3-(2-nitro-4-(trifluoromethyl)phenyl)propanoate
  参考文献：
  名称：

  Reductive Cyclizations of Nitroarenes to Hydroxamic Acids by Visible Light Photoredox Catalysis

  摘要：

  We have developed a photocatalytic reduction of nitroarenes as an efficient, chemoselective route to biologically important N-phenyl hydroxamic acid scaffolds. Optimal conditions call for 2.5 mol% of a ruthenium photocatalyst, visible light irradiation, and a dihydropyridine terminal reductant. Because of the mild nature of the visible light activation, functional groups that might be sensitive to other non-photochemical reduction methods are easily tolerated.

  DOI：

  10.1055/s-0033-1338419

文献信息

• Deconstructive di-functionalization of unstrained, benzo cyclic amines by C–N bond cleavage using a recyclable tungsten catalyst
  作者：Yujing Zhang、Shuai Sun、Yijin Su、Jian Zhao、Yong-Hong Li、Bo Han、Feng Shi

  DOI：10.1039/c9ob00693a

  日期：——

  the C–N bond in unstrained, benzo cyclic amines to generate an ester group and nitro group simultaneously. The preliminary mechanistic studies suggested that the corresponding hydroxamic acid is the key intermediate for this transformation. Importantly, with the utilization of this transformation, we achieved an interesting approach for the ring contraction of quinoline to indole, an example of scaffold

  以H 2 WO 4为催化剂，H 2 O 2为氧化剂，我们在本文中报道了在未应变的苯并环胺中C–N键的解构二官能化，可同时生成酯基和硝基。初步的机理研究表明，相应的异羟肟酸是该转化的关键中间体。重要的是，利用这种转化，我们实现了一种有趣的方法，将喹啉环缩为吲哚，这是杂芳族体系中支架跳跃的一个例子。