3-((4-chlorophenyl)amino)-3-(4-methoxyphenyl)-1-phenylpropan-1-one | 96171-57-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: 3-((4-chlorophenyl)amino)-3-(4-methoxyphenyl)-1-phenylpropan-1-one
• 英文别名: 3-(4-Chloroanilino)-3-(4-methoxyphenyl)-1-phenylpropan-1-one
• CAS: 96171-57-2
• 化学式: C₂₂H₂₀ClNO₂
• 分子量: 365.859
• InChiKey: PGQGLCGCMBPMPJ-UHFFFAOYSA-N

物化性质

• 熔点：
  117-118 °C(Solv: ethanol (64-17-5); acetone (67-64-1))
• 沸点：
  551.4±50.0 °C(Predicted)
• 密度：
  1.224±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  26
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-((4-chlorophenyl)amino)-3-(4-methoxyphenyl)-1-phenylpropan-1-one 、 2-(三甲基硅)苯基三氟甲烷磺酸盐 在 potassium fluoride 、 18-冠醚-6 作用下， 以 乙腈 为溶剂， 反应 5.0h， 以53%的产率得到1-(4-chlorophenyl)-2-(4-methoxyphenyl)-4-phenyl-1,2,3,4-tetrahydroquinolin-4-ol
  参考文献：
  名称：

  Diastereoselective Synthesis of N-Aryl Tetrahydroquinolines and N-Aryl Indolines by the Tandem Reaction of Arynes

  摘要：

  A tandem reaction of arynes with α- or β-amino ketones has been revealed. Arynes react with β-amino ketones through a cascade insertion-cyclization process to afford N-aryl tetrahydroquinolines in good yield with excellent anti-selectivity. Meanwhile, the coupling of arynes with α-amino ketones produces multisubstituted indolines in high yield with syn-selectivity. A quaternary carbon center can be constructed in this process, and the reaction can be easily scaled up.

  DOI：

  10.1021/jo5003399
• 作为产物：
  描述：

  苯乙酮 在 alkylphenylsulfonic acid functionalized silica coated magnetic Fe₃O₄ nanoparticle 作用下， 以 乙醇 为溶剂， 反应 1.5h， 生成 3-((4-chlorophenyl)amino)-3-(4-methoxyphenyl)-1-phenylpropan-1-one
  参考文献：
  名称：

  A magnetic solid sulfonic acid modified with hydrophobic regulators: an efficient recyclable heterogeneous catalyst for one-pot aza-Michael-type and Mannich-type reactions of aldehydes, ketones, and amines

  摘要：

  Two convenient green protocols for the synthesis of 3-amino ketones have been developed which involve one-pot aza-Michael-type and Mannich-type reactions of a series of aldehydes, ketones, and amines in the presence of a catalytic amount of the magnetic solid sulfonic acid catalyst, Fe3O4@SiO2@Me&Et-PhSO3H, at room temperature. The catalyst can be reused four times without loss of activity. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2015.02.088

文献信息

• Brønsted acidic ionic liquids of aza-crown ether complex cations: preparation and applications in organic reactions
  作者：Chen Cheng、Huanwang Jing

  DOI：10.1039/c4ra03061c

  日期：——

  of an aza-crown ether chelated potassium cation and various anions, were designed, synthesized and characterised by FTIR, NMR and mass spectrometry, thermogravimetric differential thermal analysis (TG-DTA) and elemental analysis. These new Brønsted acidic ionic liquids of aza-crown ether complex cations (aCBAILs) were applied as catalysts to the Biginelli reaction, Mannich reaction and synthesis of

  设计了一系列由氮杂-冠醚螯合的钾阳离子和各种阴离子组成的新型布朗斯台德酸性离子液体，并通过FTIR，NMR和质谱，热重差热分析（​​TG-DTA）和元素分析对其进行了表征。这些新的氮杂-冠醚络合物阳离子的布朗斯台德酸性离子液体（aCBAILs）被用作Biginelli反应，Mannich反应和双-（4-羟基香豆素-3-基）甲烷合成的催化剂。在温和的反应条件下，这些有机反应以高收率实现。而且，这些新的IL催化剂可以循环使用多次。
• Highly Efficient One-Pot, Three-Component Synthesis of β-Aminoketones Catalyzed by Fe(O₂CCF₃)₃
  作者：Min Zhang、Biao Xiong、Wei Yang、Ling Chen、Feng Wu、Quan Wang、Yuqiang Ding

  DOI：10.1080/00397911.2011.569866

  日期：2012.10

  Abstract A highly efficient one-pot, three-component synthesis of β-aminoketones was demonstrated using the cost-effective, noncorrosive, and easily available Fe(O2CCF3)3 as a catalyst for the first time. The method can be employed to synthesize a wide range of target compounds and to introduce different functional groups into the β-aminoketone skeleton. Additionally, the method consistently has the

  摘要 首次使用具有成本效益、无腐蚀性且易得的 Fe(O2CCF3)3 作为催化剂，证明了一种高效的一锅三组分 β-氨基酮合成方法。该方法可用于合成范围广泛的目标化合物并将不同的官能团引入β-氨基酮骨架。此外，该方法始终具有收率好、反应时间短、实验后处理简单等优点，是合成功能化β-氨基酮的有效方法。图形概要
• Pronounced Catalytic Effect of a Micellar Solution of Sodium Dodecylsulfate (SDS) Upon a Three-Component Reaction of Aldehydes, Amines, and Ketones Under Neutral Conditions
  作者：Abbas Ali Jafari、Fatemeh Moradgholi、Fatemeh Tamaddon

  DOI：10.1002/ejoc.200801037

  日期：2009.3

  A micellar solution of anionic, cationic or neutral surfactants can be used as an excellent medium for three-component Mannich reactions of aldehydes, amines, and ketones at room temperature. Sodium dodecylsulfate turned out to efficiently catalyze the reaction in neutral pure water (pH ≈ 7), and the corresponding desired β-amino ketones precipitate while the reactions proceedes. This method provides

  阴离子、阳离子或中性表面活性剂的胶束溶液可用作醛、胺和酮在室温下进行三组分曼尼希反应的优良介质。结果证明十二烷基硫酸钠在中性纯水 (pH ≈ 7) 中有效催化反应，并且在反应进行时相应的所需 β-氨基酮沉淀。该方法在温和的反应条件、干净的反应曲线、提高的产率和优异的区域选择性和非对映选择性方面提供了一种新的改进的三组分曼尼希反应，后处理简单。观察到在水中中性条件下点击化学的有趣例子。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
• Bi(NO3)3•5H2O: An Efficient and Green Catalyst for Synthesis of 1,5-Benzodiazepines and b-Amino Carbonyl Compounds
  作者：Jaspreet Kaur Rajput、Gagandeep Kaur

  DOI：10.14233/ajchem.2013.14353

  日期：——

  Bismuth nitrate pentahydrate is found to be an efficient catalyst for the synthesis of 1,5-benzodiazepines and b-amino carbonyl compounds using condensation of o-phenylenediamine with ketones and one pot three component Mannich reaction, respectively under solvent free conditions at room temperature. This method offers a simple, solvent free, room temperature, environment friendly synthesis of 1,5-benzodiazepines and b-amino carbonyl compounds. The products are isolated by column chromatography and recrystallization, respectively and were characterized by their melting point, IR and 1H NMR spectroscopy.

  五水合硝酸铋被发现是一种高效的催化剂，可在无溶剂、室温条件下分别通过邻苯二胺与酮的缩合反应以及一锅法三组分曼尼希反应合成1,5-苯二氮杂卓和β-氨基羰基化合物。这种方法提供了一种简单、无溶剂、室温、环境友好的合成1,5-苯二氮杂卓和β-氨基羰基化合物的方式。产物分别通过柱层析和重结晶进行分离，并利用熔点、红外光谱和核磁共振氢谱进行表征。
• H5CoW12O40@nanosilica: a green, bifunctional, heterogeneous nanocatalyst for one-pot three-component Mannich reaction in water
  作者：Ezzat Rafiee、Masoud Kahrizi

  DOI：10.1007/s11164-013-1392-9

  日期：2015.5

  12-Tungestocobaltic acid, H5CoW12O40, was immobilized on nanosilica from rice husk ash to produce H5CoW12O40@nanosilica as a bifunctional nanocatalyst. The TEM result showed that the particles are mostly spherical in shape, and that they have an average size of approximately 10 nm. The catalytic activity of this catalyst was investigated in Mannich reaction of various aldehydes, ketones, and amines in water. This rapid procedure afforded structurally diverse β-amino ketones in high to excellent yields. Short reaction time, simple work-up procedure, elimination of toxic solvents, and low catalyst loading are the advantages of this procedure.

  十二钨钴酸H5CoW12O40被固定在稻壳灰纳米硅上，制备出H5CoW12O40@纳米硅作为一种双功能纳米催化剂。透射电镜结果显示，这些粒子大多呈球形，平均尺寸约为10 nm。该催化剂在各种醛、酮和胺在水相中的Mannich反应中的催化活性得到了研究。这一快速过程以高至优异的产率提供了结构多样的β-氨基酮。短反应时间、简单的后处理步骤、消除有毒溶剂和低催化剂用量是这个方法的优点。