N-(bis(4-fluorophenyl)methyl)benzamide | 1135493-65-0

• 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: N-(bis(4-fluorophenyl)methyl)benzamide
• 英文别名: N-[bis(4-fluorophenyl)methyl]benzamide
• CAS: 1135493-65-0
• 化学式: C₂₀H₁₅F₂NO
• 分子量: 323.342
• InChiKey: XRFPLCLCCHTOCS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4,4'-二氟二苯甲醇 、 苯甲酰胺 在 bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] 作用下， 以 neat (no solvent) 为溶剂， 反应 3.0h， 以65%的产率得到N-(bis(4-fluorophenyl)methyl)benzamide
  参考文献：
  名称：

  无溶剂，无碱的微波介导的铱与醇的铱催化N-烷基化

  摘要：

  摘要 已经开发了无溶剂，无碱的微波介导的（Cp * IrCl 2）2催化的酰胺与醇的N-烷基化条件。已显示出一系列伯醇和仲醇可产生高产率的N-烷基芳基酰胺和N-烷基烷基酰胺。 已经开发了无溶剂，无碱的微波介导的（Cp * IrCl 2）2催化的酰胺与醇的N-烷基化条件。已显示出一系列伯醇和仲醇可产生高产率的N-烷基芳基酰胺和N-烷基烷基酰胺。

  DOI：

  10.1055/s-0033-1340142

文献信息

• Manganese(<scp>iii</scp>) acetate catalyzed oxidative amination of benzylic C(sp³)–H bonds with nitriles
  作者：Yaxing Zhang、Jianyu Dong、Lixin Liu、Long Liu、Yongbo Zhou、Shuang-Feng Yin

  DOI：10.1039/c7ob00512a

  日期：——

  Mn-Catalyzed oxidative amination of benzylic C(sp3)–H bonds with nitriles is disclosed, which enables the synthesis of a broad range of secondary amides in moderate to excellent yields under mild conditions. The interaction between Mn(III) and DDQ facilitates the oxidation and makes it highly efficient and selective.

  Mn催化的苄基C（sp 3）-H键与腈的锰催化氧化胺化反应，可在温和条件下以中等至极好的收率合成各种仲酰胺。Mn（III）与DDQ之间的相互作用促进了氧化，使其变得高效且具有选择性。
• <i>o</i>-Benzenedisulfonimide as a Reusable Brønsted Acid Catalyst for Ritter-Type Reactions
  作者：Margherita Barbero、Stefano Bazzi、Silvano Cadamuro、Stefano Dughera

  DOI：10.1002/ejoc.200800931

  日期：2009.1

  Reactions between various benzyl alcohols or tert-butyl alcohol and nitriles were carried out in the presence of catalytic amounts (usually 10–20 mol-%) of o-benzenedisulfonimide as a Bronsted acid catalyst; the reaction conditions were mild and the yields of amides were good. The catalyst was easily recovered and purified, ready to be used in further reactions, with economic and ecological advantages

  各种苯甲醇或叔丁醇与腈之间的反应是在催化量（通常为 10-20 mol%）的邻苯二磺酰亚胺作为布朗斯台德酸催化剂存在下进行的。反应条件温和，酰胺收率良好。该催化剂易于回收和纯化，可用于进一步的反应，具有经济和生态优势。（© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009）
• Au(iii)-catalyzed intermolecular amidation of benzylic C–H bonds
  作者：Yan Zhang、Bainian Feng、Chengjian Zhu

  DOI：10.1039/c2ob26857d

  日期：——

  Au(III)-catalyzed intermolecular amidations of benzylic C–H bonds with sulfonamides and carboxamides are described. The protocol with the Au–bipy complex/N-bromosuccinimide system provides practical applications for synthesis of various amides via C–H activations. The reaction proceeds with high efficiency to give the corresponding amines, which are extremely useful synthetic intermediates.

  描述了金（III）催化的苄基CH键与磺酰胺和羧酰胺的分子间酰胺化反应。Au-bipy配合物/ N-溴代琥珀酰亚胺系统的协议为通过CH活化合成各种酰胺提供了实际应用。反应以高效率进行，得到相应的胺，它们是非常有用的合成中间体。
• An expedient, efficient and solvent-free synthesis of T3P®-mediated amidation of benzhydrols with poorly reactive N-nucleophiles under MW irradiation
  作者：Srinivas Cheruku、Sandhya C. Nagarakere、Makanahalli P. Sunilkumar、Yatheesh Narayana、Kumara N. Manikyanally、Kanchugarakoppal S. Rangappa、Kempegowda Mantelingu

  DOI：10.1039/d1nj04502d

  日期：——

  An expedient, efficient, economical, environmentally benign, and solvent free amidation protocol of benzhydrols with less reactive nitrogen nucleophiles assisted by propylphosphonic anhydride (T3P®) under microwave irradiation has been developed. The methodology has been deployed for a wide range of heterocycles and electron-withdrawing & electron-donating groups. The protocol resulted in good to excellent

  已经开发了一种方便、高效、经济、环境友好且无溶剂的苯甲醇与低活性氮亲核试剂的酰胺化方案，该方案在微波辐射下由丙基膦酸酐 (T3P®) 辅助。该方法已应用于广泛的杂环和吸电子和给电子基团。该协议在给定条件下产生了良好的产量（26 个示例，68-93% 的产量）。