(4-methoxy-1H-indol-3-yl)(phenyl)methanone | 1315590-48-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: (4-methoxy-1H-indol-3-yl)(phenyl)methanone
• 英文别名: (4-methoxy-1H-indol-3-yl)-phenylmethanone
• CAS: 1315590-48-7
• 化学式: C₁₆H₁₃NO₂
• mdl: MFCD25308939
• 分子量: 251.285
• InChiKey: KRZBEQSYJLUBOW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.062
• 拓扑面积：
  42.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-甲氧基吲哚 、 苯甲基苯胺 在 叔丁基过氧化氢 、 三甲基丙酮酸 、 2,3-二氯-5,6-二氰基-1,4-苯醌 、 iron(II) chloride 作用下， 以 癸烷 、 二甲基亚砜 为溶剂， 反应 24.0h， 以53%的产率得到(4-methoxy-1H-indol-3-yl)(phenyl)methanone
  参考文献：
  名称：

  Mild and Selective Ru-Catalyzed Formylation and Fe-Catalyzed Acylation of Free (N–H) Indoles Using Anilines as the Carbonyl Source

  摘要：

  C3-selective formylation and acylation of free (N-H) indoles under mild conditions can be achieved by using Ru- and Fe-catalyzed oxidative coupling of free (N-H) indoles with anilines, respectively. Both processes are operationally simple, compatible with a variety of functional groups and generally provide the desired products in good yields. (13)C-labeling experiments unambiguously established that the carbonylic carbon in the formylation products originated from methyl group of N-methyl aniline.

  DOI：

  10.1021/ja2048495

文献信息

• Decarboxylative acylation of <i>N</i>-free indoles enabled by a catalytic amount of copper catalyst and liquid-assisted grinding
  作者：Jingbo Yu、Chao Zhang、Xinjie Yang、Weike Su

  DOI：10.1039/c9ob00622b

  日期：——

  A facile decarboxylative acylation of N-free indoles with α-ketonates via liquid-assisted grinding was reported. The reaction requires only a catalytic amount of Cu(OAc)2·H2O in combination with O2 as the terminal oxidant to give various 3-acylindoles with high efficiency. Additionally, this new methodology was applicable to a gram-scale synthesis.

  报道了通过液体辅助研磨将无氮吲哚与α-酮类化合物容易地脱羧酰化。该反应仅需要催化量的Cu（OAc）2 ·H 2 O与作为末端氧化剂的O 2结合就可以高效地得到各种3-酰基环。此外，这种新方法适用于克级合成。
• Mild and Selective Ru-Catalyzed Formylation and Fe-Catalyzed Acylation of Free (N–H) Indoles Using Anilines as the Carbonyl Source
  作者：Wenliang Wu、Weiping Su

  DOI：10.1021/ja2048495

  日期：2011.8.10

  C3-selective formylation and acylation of free (N-H) indoles under mild conditions can be achieved by using Ru- and Fe-catalyzed oxidative coupling of free (N-H) indoles with anilines, respectively. Both processes are operationally simple, compatible with a variety of functional groups and generally provide the desired products in good yields. (13)C-labeling experiments unambiguously established that the carbonylic carbon in the formylation products originated from methyl group of N-methyl aniline.