4-[(4-chlorophenyl)(1H-indol-3-yl)methyl]-N,N-dimethylaniline | 1307875-32-6

• 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: 4-[(4-chlorophenyl)(1H-indol-3-yl)methyl]-N,N-dimethylaniline
• 英文别名: 4-[(4-chlorophenyl)-(1H-indol-3-yl)methyl]-N,N-dimethylaniline
• CAS: 1307875-32-6
• 化学式: C₂₃H₂₁ClN₂
• 分子量: 360.886
• InChiKey: GFKZKSAIJJMVBM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  19
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  吲哚 、 4-氯苯甲醛 、 N,N-二甲基苯胺 在 zinc(II) chloride 作用下， 以 甲苯 为溶剂， 反应 5.0h， 以68%的产率得到4-[(4-chlorophenyl)(1H-indol-3-yl)methyl]-N,N-dimethylaniline
  参考文献：
  名称：

  ZnCl 2促进了3-芳基甲基和二芳基甲基吲哚的高效一锅合成

  摘要：

  无水ZnCl 2介导的方便，一锅法合成3-芳基甲基和二芳基甲基吲哚的收率很高。在反应条件下，原位形成了动力学上稳定的双（吲哚基）甲烷产物。通过与双（吲哚基）甲烷进行压力管反应，证实了其随后在升高的温度和压力下转化为热力学稳定的3-二芳基甲基吲哚。

  DOI：

  10.1016/j.tetlet.2013.11.115

文献信息

• Strong Lewis acid air-stable cationic titanocene perfluoroalkyl(aryl)sulfonate complexes as highly efficient and recyclable catalysts for C–C bond forming reactions
  作者：Ningbo Li、Jinying Wang、Xiaohong Zhang、Renhua Qiu、Xie Wang、Jinyang Chen、Shuang-Feng Yin、Xinhua Xu

  DOI：10.1039/c4dt00549j

  日期：——

  A series of titanocene perfluoroalkyl(aryl)sulfonate complexes were synthesized, characterized, and applied in various C–C bond forming reactions.

  一系列的钛ocene基过氟烷基（芳基）磺酸盐配合物被合成、表征，并应用于各种C-C键形成反应。
• FeCl3 as Lewis acid catalyzed one-pot three-component aza-Friedel–Crafts reactions of indoles, aldehydes, and tertiary aromatic amines
  作者：Jie Liu、Tao He、Lei Wang

  DOI：10.1016/j.tet.2011.03.050

  日期：2011.5

  A new strategy for the synthesis of 3-diarylmethyl indoles was developed through FeCl3 as Lewis acid catalyzed three-component aza-Friedel–Crafts reactions of indoles, aldehydes, and tertiary aromatic amines in one-pot. The reactions generated the corresponding 3-diarylmethyl indoles in good yields under mild reaction conditions by using less expensive, readily available, and environmentally benign

  通过路易斯酸催化一锅合成吲哚，醛和叔芳族胺的三组分氮杂-弗里德尔-克来夫特反应，通过FeCl 3提出了一种新的3-二芳基甲基吲哚合成策略。通过使用较便宜，易于获得且对环境无害的铁催化剂，该反应在温和的反应条件下以高收率产生了相应的3-二芳基甲基吲哚。重要的是要注意，此反应的关键特征是操作简便。
• Three-component synthesis of 3-(diarylmethyl)indoles using Fe(ClO4)3/SiO2 as catalyst
  作者：E. Najafi、F. K. Behbahani

  DOI：10.1134/s107042801703023x

  日期：2017.3

  Three-component reaction of indole, aromatic aldehyde, and N,N-dimethyl aniline in the presence of silica-supported Fe(ClO4)3 as catalyst afforded the corresponding 3-[aryl(4-dimethylaminophenyl)methyl]-indoles in excellent yields under mild conditions. The proposed protocol offers some remarkable advantages such as the use of a solid catalyst and simple workup procedure.

  在二氧化硅负载的Fe（ClO 4）3作为催化剂的存在下，吲哚，芳族醛和N，N-二甲基苯胺的三组分反应得到相应的3- [芳基（4-二甲基氨基苯基）甲基]吲哚，在温和条件下的产量。所提出的方案具有一些显着的优点，例如使用固体催化剂和简单的后处理程序。
• Brønsted Acidic Ionic Liquid Catalyzed Three-Component Friedel–Crafts Reaction for the Synthesis of Unsymmetrical Triarylmethanes
  作者：Uthaiwan Sirion、Suttida Rinkam、Warapong Senapak、Sarayut Watchasit、Rungnapha Saeeng

  DOI：10.1055/a-1809-7768

  日期：2022.9

  A convenient and practical method for the synthesis of unsymmetrical triarylmethanes was demonstrated through a one-pot three-component double Friedel–Crafts reaction of various aliphatic, aromatic, or heteroaromatic aldehydes with N,N-dialkylanilines and indoles by using a Brønsted acidic ionic liquid as the catalyst. This method was successfully applied under metal- and solvent-free conditions at

  通过使用布朗斯台德酸性离子液体，各种脂肪族、芳香族或杂芳香族醛与N , N - 二烷基苯胺和吲哚的一锅三组分双傅克反应，证明了一种方便实用的合成不对称三芳基甲烷的方法作为催化剂。该方法在 80 °C 的无金属和无溶剂条件下成功应用，从广泛的底物中以中等至高产率提供了相应的不对称三芳基甲烷产物。此外，通过定量NMR分析研究了该反应的机理。
• PMA-SiO₂–Mediated MCR in PEG-400: A Greener aza-Friedel–Crafts Reaction Leading to 3-Arylmethyl/Diarylmethyl Indoles
  作者：Dinne Naresh Kumar Reddy、Kothapalli Bannoth Chandrasekhar、Yaddanapudi Sesha Siva Ganesh、Srikanth Sharathchandra Gorantla、Siddabathuni Ramanjaneyulu、K. Shiva Kumar、Manojit Pal

  DOI：10.1080/00397911.2014.966392

  日期：2015.2.16

  A greener approach for the synthesis of 3-arylmethyl/diarylmethyl indoles has been achieved via a PMA-SiO2-mediated three-component reaction (the aza-Friedel-Crafts reaction) involving indoles, aldehydes, and N,N-disubstituted anilines in PEG-400. A variety of indole derivatives were prepared by using this operationally simple and straightforward methodology in acceptable yields.