phenyl 4-(diphenylamino)benzoate | 1432623-62-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 缩酚酸和缩酚酸环醚类
• 英文名称: phenyl 4-(diphenylamino)benzoate
• 英文别名: phenyl 4-(N-phenylanilino)benzoate
• CAS: 1432623-62-5
• 化学式: C₂₅H₁₉NO₂
• 分子量: 365.431
• InChiKey: OADMTEZCVSQHIK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  29.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  phenyl 4-(diphenylamino)benzoate 在 三氟甲磺酸 作用下， 反应 19.0h， 以76%的产率得到(4-(diphenylamino)phenyl)(2-hydroxyphenyl)methanone
  参考文献：
  名称：

  Paraphenylene dimers with diphenylamine donor groups: synthesis and photophysics

  摘要：

  A novel paraphenylene dimer (D696) with electron donating diphenylamine side chain groups has been prepared. Optical absorption measurements were theoretically and experimentally determined showing a red shift in the absortivity relative to dialkylamine functionalized benzophenone dimers. The fluorescence of D696 was quenched in a concentration dependent manner in the presence of reduced graphene oxide (RGO). (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.03.141
• 作为产物：
  描述：

  二苯胺 在 4-二甲氨基吡啶 、 palladium diacetate 、 caesium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 、 N,N'-二环己基碳二亚胺 、 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 36.0h， 生成 phenyl 4-(diphenylamino)benzoate
  参考文献：
  名称：

  Paraphenylene dimers with diphenylamine donor groups: synthesis and photophysics

  摘要：

  A novel paraphenylene dimer (D696) with electron donating diphenylamine side chain groups has been prepared. Optical absorption measurements were theoretically and experimentally determined showing a red shift in the absortivity relative to dialkylamine functionalized benzophenone dimers. The fluorescence of D696 was quenched in a concentration dependent manner in the presence of reduced graphene oxide (RGO). (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.03.141

文献信息

• Ester Transfer Reaction of Aromatic Esters with Haloarenes and Arenols by a Nickel Catalyst
  作者：Ryota Isshiki、Naomi Inayama、Kei Muto、Junichiro Yamaguchi

  DOI：10.1021/acscatal.0c00291

  日期：2020.3.6

  transfer reaction of aromatic esters with aryl halides/arenols was developed. The present reaction can transfer an ester functional group from certain aromatic esters to haloarenes. This ester transfer reaction involves two oxidative additions—one from the C–C bond of the aromatic ester and one from the C–halogen bond of haloarenes—onto a nickel catalyst. The utilization of a Ni/dcypt catalyst capable

  开发了芳族酯与芳基卤化物/芳烃的催化酯转移反应。本反应可以将酯官能团从某些芳族酯转移至卤代芳烃。这种酯转移反应涉及到镍催化剂上的两种氧化加成反应（一种是芳香族酯的C–C键，另一种是卤代芳烃的C–卤素键）。使用能够裂解两个化学键的Ni / dcypt催化剂是反应进展的关键。此外，基于萘酚的芳基亲电试剂也可通过C–O键活化而应用于催化体系。
• METHOD FOR PRODUCING ORGANIC COMPOUND AND ORGANIC COMPOUND OBTAINED BY THE METHOD
  申请人：Enomura Masakazu

  公开号：US20110178199A1

  公开（公告）日：2011-07-21

  Disclosed herein are a reaction method and a production method of an organic compound which are capable of achieving high reaction selectivity according to the purpose and a high production rate of a target substance. The methods include at least two fluids, wherein at least one kind of the fluids is a fluid containing at least one organic compound and at least one kind of the fluids other than the above fluid is a fluid containing at least one reactant in the form of a liquid or solution, and the respective fluids join together in a thin film fluid foamed between processing surfaces arranged to be opposite to each other so as to be able to approach to and separate from each other, at least one of which rotates relative to the other, whereby an organic reaction is performed in the thin film fluid.

  本文公开了一种有机化合物的反应方法和生产方法，能够根据目的实现高反应选择性和目标物质的高产率。该方法包括至少两种流体，其中至少一种流体是含有至少一种有机化合物的流体，除上述流体外的至少一种流体是以液态或溶液形式含有至少一种反应物的流体。这些各自的流体在处理表面之间形成一个薄膜流体泡沫，这些处理表面相对排列以便能够相互接近和分离，其中至少有一个表面相对于另一个表面旋转，从而在薄膜流体中进行有机反应。