N-(4-chlorobenzyl)-N-phenylacetamide | 68014-56-2

• 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-(4-chlorobenzyl)-N-phenylacetamide
• 英文别名: N-(4-chlorophenyl)-N-phenylacetamide；N-Acetyl-4-chlor-diphenylamin
• CAS: 68014-56-2
• 化学式: C₁₄H₁₂ClNO
• 分子量: 245.708
• InChiKey: DWYPLEWYGABZQP-UHFFFAOYSA-N

物化性质

• 沸点：
  456.2±28.0 °C(Predicted)
• 密度：
  1.231±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N-(4-chlorobenzyl)-N-phenylacetamide 在 palladium diacetate 、 溶剂黄146 、 silver(l) oxide 作用下， 以60%的产率得到3-chloro-N-acetylcarbazole
  参考文献：
  名称：

  Pd(II)-catalyzed intramolecular C–H activation/C–C cross coupling for the synthesis of carbazoles from diaryl acetamides

  摘要：

  Pd(II)-catalyzed intramolecular C-H activation/C-C cross coupling within N,N-diphenyl-acetamides allows the efficient formation of differently substituted carbazoles. In this cross-dehydrogenative coupling, many different functional groups are tolerated and the starting material N,N-diphenyl-acetamides can be easily prepared in one step from commercially available acetanilides and iodobenzenes. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.11.082
• 作为产物：
  描述：

  对氯苯胺 在 molecular sieve 、 三氟化硼乙醚 、 间氯过氧苯甲酸 作用下， 以 氯仿 为溶剂， 反应 1.0h， 生成 N-(4-chlorobenzyl)-N-phenylacetamide
  参考文献：
  名称：

  Kim, So Yeon; An, Gwang-Il; Rhee, Hakjune, Synlett, 2003, # 1, p. 112 - 114

  摘要：

  DOI：

文献信息

• Transition metal-free N-arylation of secondary amides through iodonium salts as aryne precursors
  作者：Ming Wang、Zhijian Huang

  DOI：10.1039/c6ob01649a

  日期：——

  By using a diaryliodonium salt as a benzyne precursor, a transition metal-free approach for N-arylation of secondary amides is developed. This novel benzyne precursor, which can be prepared easily by a one step process from an aryl iodide, shows different reactivities with previous benzyne precursors in the N-arylation reaction. Mechanistic studies confirm the involvement of benzyne species (generated

  通过使用二芳基碘鎓盐作为苯并炔前体，开发了无过渡金属的仲酰胺N-芳基化方法。可以通过一步法由芳基碘化物容易地制备的这种新型苯并炔前体在N-芳基化反应中显示出与先前的苯并炔前体不同的反应性。机理研究证实，苯并炔物种（由二芳基碘鎓盐原位生成）作为关键中间体参与其中。
• 一种高价碘试剂介导的氯苯对位胺化化合物的制备方法
  申请人：湖北工业大学

  公开号：CN113248396B

  公开（公告）日：2023-03-14

  本发明涉及一种高价碘试剂介导的氯苯对位胺化化合物的制备方法，包括下列步骤：按先后顺序向反应器中加入取代乙酰苯胺、对氯碘苯二乙酯、氯苯、六氟异丙醇和磁子，将反应器置于20℃～40℃油浴锅中搅拌反应2‑6小时，终止反应，提纯产物得到氯苯对位胺化化合物。本发明反应条件温和、选择性高、产率较高及对环境友好，合成的氯苯对位胺化化合物具有较好的生物活性，可以应用到药物合成、农药合成以及涂料染料合成等领域。
• BIPYRIDINE COMPOUND, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCTION OF CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX
  申请人：Asaumi Taku

  公开号：US20100184978A1

  公开（公告）日：2010-07-22

  A bipyridine compound represented by the formula (1): wherein R 1 , R 2 and R 3 each independently represent a C1-C10 alkyl group which may be substituted etc., and R 4 , R 5 , R 6 , R 7 and R 8 each independently represent a hydrogen atom etc., a transition metal complex obtained by contacting a bipyridine compound represented by the formula (1) with a compound of a transition metal belonging to Group 9, 10 or 11, and a method for production of a conjugated aromatic compound comprising reacting an aromatic compound (A) wherein one or two leaving groups are bonded to an aromatic ring with an aromatic compound (A) having the same structure as that of the above-mentioned aromatic compound (A) or an aromatic compound (B) being structurally different from the above-mentioned aromatic compound (A) and having one or two leaving groups bonded to an aromatic ring, in the presence of the transition metal complex.

  一种以式(1)表示的联吡啶化合物：其中R1、R2和R3各自独立地表示可以被取代的C1-C10烷基等，而R4、R5、R6、R7和R8各自独立地表示氢原子等，通过将式(1)表示的联吡啶化合物与属于9、10或11族过渡金属的化合物接触而获得的过渡金属配合物，以及一种制备共轭芳香化合物的方法，包括在过渡金属配合物的存在下，将一个或两个离去基团与芳环结合的芳香化合物（A）与具有与上述芳香化合物（A）相同结构的芳香化合物（A）或结构不同于上述芳香化合物（A）且具有一个或两个离去基团与芳环结合的芳香化合物（B）反应。
• TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX
  申请人：Asaumi Taku

  公开号：US20110046336A1

  公开（公告）日：2011-02-24

  A transition metal complex obtained by contacting a bipyridine compound represented by the formula (1): wherein R 1 , R 2 and R 3 represent a C1-C10 alkyl group which may be substituted, etc., and R 4 and R 5 represent a hydrogen atom etc., with a compound of a transition metal belonging to Group 9, 10 or 11, and a process for producing a conjugated aromatic compound comprising reacting an aromatic compound (A) wherein one or two leaving groups are bonded to an aromatic ring with an aromatic compound (A) having the same structure as that of the above-mentioned aromatic compound (A) or an aromatic compound (B) being structurally different from the above-mentioned aromatic compound (A) and having one or two leaving groups bonded to an aromatic ring, in the presence of said transition metal complex.

  通过将式（1）所表示的联吡啶化合物与属于9、10或11族的过渡金属化合物接触而获得的过渡金属配合物，其中R1、R2和R3代表C1-C10烷基，可以被取代等，而R4和R5代表氢原子等。制备共轭芳香化合物的方法包括，在所述过渡金属配合物的存在下，将一个芳香化合物（A），其中一个或两个离去基团与芳香环相键合，与具有与上述芳香化合物（A）相同结构的芳香化合物（A）或在结构上不同于上述芳香化合物（A）并且具有一个或两个离去基团与芳香环相键合的芳香化合物（B）反应。
• Exploiting the Marcus inverted region for first-row transition metal–based photoredox catalysis
  作者：Amy Y. Chan、Atanu Ghosh、Jonathan T. Yarranton、Jack Twilton、Jian Jin、Daniela M. Arias-Rotondo、Holt A. Sakai、James K. McCusker、David W. C. MacMillan

  DOI：10.1126/science.adj0612

  日期：2023.10.13

  Second- and third-row transition metal complexes are widely employed in photocatalysis, whereas earth-abundant first-row transition metals have found only limited use because of the prohibitively fast decay of their excited states. We report an unforeseen reactivity mode for productive photocatalysis that uses cobalt polypyridyl complexes as photocatalysts by exploiting Marcus inverted region behavior

  第二和第三行过渡金属络合物广泛应用于光催化，而地球上丰富的第一行过渡金属由于其激发态的快速衰减而仅具有有限的用途。我们报告了一种不可预见的高效光催化反应模式，该模式利用钴聚吡啶配合物作为光催化剂，利用马库斯倒置区域行为，将激发态能量的增加与激发态寿命的增加结合起来。这些钴 (III) 配合物凭借其强大的氧化还原电位和足够长的激发态寿命可以参与双分子反应，催化氧化 C(sp 2 )–芳基酰胺与具有挑战性的位阻芳基硼酸的 N 偶联。更一般地说，结果意味着发色团可以设计为增加激发态寿命，同时增加激发态能量，为使用相对丰富的金属作为光氧化还原催化剂提供了途径。