3-氯-N-(3-氯苯基)苯胺 | 32113-77-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-氯-N-(3-氯苯基)苯胺
• 英文名称: 3,3'-dichlorodiphenylamine
• 英文别名: Di-(3-chlorphenyl)-amin；bis-(3-chloro-phenyl)-amine；Bis-(3-chlor-phenyl)-amin；Diphenylamine, 3,3'-dichloro-；3-chloro-N-(3-chlorophenyl)aniline
• CAS: 32113-77-2
• 化学式: C₁₂H₉Cl₂N
• 分子量: 238.116
• InChiKey: YVDNMDPKDNOULT-UHFFFAOYSA-N

物化性质

• 沸点：
  379.77°C (rough estimate)
• 密度：
  1.3067 (rough estimate)

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 海关编码：
  2921499090

反应信息

• 作为反应物：
  描述：

  3-氯-N-(3-氯苯基)苯胺 在 4-二甲氨基吡啶 、 正丁基锂 、 sodium hydride 、 三氟乙酸 作用下， 以 四氢呋喃 、 正己烷 、 mineral oil 为溶剂， 反应 49.5h， 生成 1,8-Dichloro-10-methylacridin-9-one
  参考文献：
  名称：

  带有1,8-二氯ac啶基部分的烯丙基化合物的氧化和卤代烯丙基化合物的光解作用，生成三重态卡宾

  摘要：

  合成了带有1,8-二氯ac啶基部分的新的丙二烯化合物5c和5d，并进行了5c和5d的氧化以生成热稳定的三重态卡宾。由于氧化导致分解产物的形成，因此进行了溴化丙二烯化合物18的光解。尽管光解效率非常低，但在低温下的紫外可见测量结果表明，中间体18的生成与起始原料18的减少有关。ESR和电子自旋瞬态章动（ESTN）光谱表明，中间体的多重性是三重态，可能是目标三重态卡宾6d生成。在...方面 D | 中间体的ESR值表明，通过在骨架中引入氮原子（方案1中的双自由基特性），未配对的电子在6d内更有效地离域。观察到的三重态物种6d不够稳定，无法分离。版权所有©2014 John Wiley＆Sons，Ltd.

  DOI：

  10.1002/poc.3398
• 作为产物：
  描述：

  N-(3-chlorophenyl)benzimidoyl chloride 、 3-氯苯酚 在 乙醚 、 sodium ethanolate 作用下， 生成 3-氯-N-(3-氯苯基)苯胺
  参考文献：
  名称：

  XXXIX.-10-Chloro-5：10-dihydrophenarsazine及其衍生物。第十四部分氯代衍生物

  摘要：

  DOI：

  10.1039/jr9310000294

文献信息

• Chan‐Evans‐Lam C−N Coupling Promoted by a Dinuclear Positively Charged Cu(II) Complex. Catalytic Performance and Some Evidence for the Mechanism of CEL Reaction Obviating Cu(III)/Cu(I) Catalytic Cycle
  作者：Nikolay Akatyev、Mikhail Il'in、Mikhail Il'in(Jr.)、Svetlana Peregudova、Alexander Peregudov、Anastasiya Buyanovskaya、Kirill Kudryavtsev、Alexander Dubovik、Valerij Grinberg、Victor Orlov、Alexander Pavlov、Valentin Novikov、Ilya Volkov、Yuri Belokon

  DOI：10.1002/cctc.202000212

  日期：2020.6.5

  molecular weight measurements of the catalytic complex in MeOH and the kinetic studies of aniline and phenylboronic acid coupling. In addition, an 1H NMR experiment in a sealed NMR tube, without external oxygen supply available, proved that no complete Cu(II) to Cu(I) conversion was observed under the condition, ruling out the usually accepted mechanism of the C−N coupling, which included the oxygenation

  在本研究中，我们报告了一系列具有广泛配体的铜（II）配合物的合成及其在铜催化苯胺和苯基硼酸的Chan-Evans-Lam（CEL）偶联中的测试。偶联的效率与配合物的Cu（II）还原为Cu（I）的容易程度直接相关。最有效的催化剂是由4-衍生吨2,5,5-双[（喹啉基亚氨基）甲基]酚丁酸酯和两个Cu（II）离子。取决于抗衡阴离子的性质和反应混合物的浓度，反应可以直接导致CN键的形成。在最佳条件下制备了43种二苯胺衍生物。所提出的催化机理是基于一系列配合物的还原电位，在甲醇中催化配合物的分子量测量以及苯胺和苯基硼酸偶联的动力学研究。另外，1在没有外部氧气供应的情况下，在密封的NMR管中进行的H NMR实验证明，在此条件下未观察到完全的Cu（II）到Cu（I）的转化，排除了通常公认的CN偶联机理，包括在完成CN转换的关键步骤后，中间形成的Cu（I）络合物的氧合作用已经完成。取而代之的是，提出了一种
• Synthesen auf dem Phenothiazin-Gebiet. 3. Mitteilung. Neue Phenothiazinderivate
  作者：J.-P. Bourquin、G. Schwarb、G. Gamboni、R. Fischer、L. Ruesch、S. Guldimann、V. Theus、E. Schenker、J. Renz

  DOI：10.1002/hlca.19590420124

  日期：——

  The synthesis and properties of various N- and C-3-substituted derivatives of phenothiazine are described.

  描述了吩噻嗪的各种N-和C-3-取代的衍生物的合成和性质。
• Process for producing compound, catalyst component for addition polymerization, process for producing catalyst for addition polymerization, and process for producing addition polymer
  申请人：Oshima Hideki

  公开号：US20050222351A1

  公开（公告）日：2005-10-06

  There are provided (1) a process for producing a compound, which comprises the step of contacting a compound (A) defined by the formula, M 1 L 1 3 , a compound (B) defined by the formula, R 1 t-1 TH, and a compound (C) defined by the formula, R 2 t-2 TH 2 ; (2) a catalyst component for addition polymerization, which comprises a compound produced by said process; (3) a process for producing a polymerization catalyst, which comprises the step of contacting said catalyst component with a transition metal compound and an optional organoaluminum compound; and (4) a process for producing an addition polymer, which comprises the step of addition polymerizing an addition polymerizable monomer in the presence of a catalyst produced by said process.

  提供以下内容：（1）生产化合物的过程，包括将由M1L13公式定义的化合物（A）、由R1t-1TH公式定义的化合物（B）和由R2t-2TH2公式定义的化合物（C）接触的步骤；（2）用于加成聚合的催化剂组分，包括通过上述过程产生的化合物；（3）生产聚合催化剂的过程，包括将催化剂组分与过渡金属化合物和可选的有机铝化合物接触的步骤；（4）生产加成聚合物的过程，包括在上述过程产生的催化剂存在下加成聚合可聚合单体的步骤。
• TRANSITION METAL COMPOUND AND CATALYST FOR OLEFIN POLYMERIZATION
  申请人：HANAOKA Hidenori

  公开号：US20110319578A1

  公开（公告）日：2011-12-29

  A transition metal compound represented by the formula (1-1) or the formula (1-2) (M is a transition metal atom) and a process for producing a catalyst for olefin polymerization comprising a step of bringing the transition metal compound into contact with a co-catalytic component for activation.

  一种由化学式(1-1)或化学式(1-2)所代表的过渡金属化合物（其中M是一种过渡金属原子）和制备催化剂的方法，包括将该过渡金属化合物与协同催化剂成分接触以激活的步骤。
• Transition Metal Complex, Process For Producing Said Transition Metal Complex, Substituent-Carrying Fluorene Compound, Process For Producing Said Fluorene Compound, Catalyst Component For Olefin Polymerization, Catalyst For Olefin Polymerization, and Process For Producing Olefin Polymer
  申请人：Senda Taichi

  公开号：US20080161514A1

  公开（公告）日：2008-07-03

  A transition metal complex represented by the general formula [1]; a catalyst component for olefin polymerization comprising said transition metal complex; a catalyst for olefin polymerization using said transition metal complex as a catalyst component for olefin polymerization; a process for producing an olefin polymer comprising the step of polymerizing an olefin in the presence of said catalyst for olefin polymerization; a substituent-carrying fluorene compound; a process for producing said substituent-carrying fluorene compound; and a process for producing said transition metal complex using said substituent-carrying fluorene compound: wherein M is the group 4 transition metal atom in the periodic table of elements; A is the group 16 atom therein; J is the group 14 atom therein; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , X 1 and X 2 are independently of one another (1) a substituent selected from the group consisting of (1-1) an alkyl group having 1 to 20 carbon atoms, which may be substituted by a halogen atom, (1-2) an aralkyl group having 7 to 20 carbon atoms, which may be substituted by a halogen atom, (1-3) an aryl group having 6 to 20 carbon atoms, which may be substituted by a halogen atom, (1-4) a substituent-carrying silyl group having 1 to 20 carbon atoms, which substituent is a hydrocarbyl group, and said hydrocarbyl group may be substituted by a halogen atom, (1-5) a disubstituent-carrying amino group having 2 to 20 carbon atoms, which substituent is a hydrocarbyl group, and said hydrocarbyl group may be substituted by a halogen atom, (1-6) an alkoxy group having 1 to 20 carbon atoms, which may be substituted by a halogen atom, (1-7) an aralkyloxy group having 7 to 20 carbon atoms, which may be substituted by a halogen atom, and (1-8) an aryloxy group having 6 to 20 carbon atoms, which may be substituted by a halogen atom, (2) a halogen atom or (3) a hydrogen atom; R 1 and R 2 , R 2 and R 3 , and R 3 and R 4 may be linked to each other, respectively, to form respective rings; R 5 and R 6 may be linked to each other to form a ring; R 7 , R 8 , R 9 and R 10 are independently of one another (1) a substituent selected from the group consisting of (1-1) an alkyl group having 1 to 20 carbon atoms, which may be substituted by a halogen atom, (1-2) an aralkyl group having 7 to 20 carbon atoms, which may be substituted by a halogen atom, (1-3) an aryl group having 6 to 20 carbon atoms, which may be substituted by a halogen atom, (1-4) a substituent-carrying silyl group having 1 to 20 carbon atoms, which substituent is a hydrocarbyl group, and said hydrocarbyl group may be substituted by a halogen atom, (1-5) a disubstituent-carrying amino group having 2 to 20 carbon atoms, which substituent is a hydrocarbyl group, and said hydrocarbyl group may be substituted by a halogen atom, (1-6) an alkoxy group having 1 to 20 carbon atoms, which may be substituted by a halogen atom, (1-7) an aralkyloxy group having 7 to 20 carbon atoms, which may be substituted by a halogen atom, and (1-8) an aryloxy group having 6 to 20 carbon atoms, which may be substituted by a halogen atom, (2) a halogen atom or (3) a hydrogen atom; at least two of R 7 , R 8 , R 9 and R 10 are the substituent selected from the above-mentioned group or a halogen atom; R 7 and R 8 may be linked to each other to form a ring; and R 9 and R 10 may be linked to each other to form a ring.

  一种以通式[1]表示的过渡金属配合物；一种包括该过渡金属配合物的烯烃聚合催化剂组分；一种使用该过渡金属配合物作为烯烃聚合催化剂组分的烯烃聚合催化剂；一种在该烯烃聚合催化剂存在下聚合烯烃的方法；一种携带取代基的芴化合物；一种制备该携带取代基的芴化合物的方法；以及一种使用该携带取代基的芴化合物制备该过渡金属配合物的方法：其中，M是元素周期表中的第4族过渡金属原子；A是其中的第16族原子；J是其中的第14族原子；R1、R2、R3、R4、R5、R6、X1和X2各自独立地是（1）选自以下组中的取代基：（1-1）具有1至20个碳原子的烷基取代基，其可以被卤素原子取代，（1-2）具有7至20个碳原子的芳基烷基取代基，其可以被卤素原子取代，（1-3）具有6至20个碳原子的芳基取代基，其可以被卤素原子取代，（1-4）携带取代基的具有1至20个碳原子的硅烷基，其取代基是烃基，且该烃基可以被卤素原子取代，（1-5）携带二个取代基的具有2至20个碳原子的氨基取代基，其取代基是烃基，且该烃基可以被卤素原子取代，（1-6）具有1至20个碳原子的烷氧基，其可以被卤素原子取代，（1-7）具有7至20个碳原子的芳基烷氧基，其可以被卤素原子取代，以及（1-8）具有6至20个碳原子的芳氧基，其可以被卤素原子取代，（2）卤素原子或（3）氢原子；R1和R2、R2和R3以及R3和R4可以分别相互连接以形成相应的环；R5和R6可以连接以形成环；R7、R8、R9和R10各自独立地是（1）选自上述组中的取代基：（1-1）具有1至20个碳原子的烷基取代基，其可以被卤素原子取代，（1-2）具有7至20个碳原子的芳基烷基取代基，其可以被卤素原子取代，（1-3）具有6至20个碳原子的芳基取代基，其可以被卤素原子取代，（1-4）携带取代基的具有1至20个碳原子的硅烷基，其取代基是烃基，且该烃基可以被卤素原子取代，（1-5）携带二个取代基的具有2至20个碳原子的氨基取代基，其取代基是烃基，且该烃基可以被卤素原子取代，（1-6）具有1至20个碳原子的烷氧基，其可以被卤素原子取代，（1-7）具有7至20个碳原子的芳基烷氧基，其可以被卤素原子取代，以及（1-8）具有6至20个碳原子的芳氧基，其可以被卤素原子取代，（2）卤素原子或（3）氢原子；R7、R8、R9和R10中至少有两个是上述组中的取代基或卤素原子；R7和R8可以连接以形成环；R9和R10可以连接以形成环。