N,N-dimethyl-3-(phenylthio)aniline | 103206-21-9

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: N,N-dimethyl-3-(phenylthio)aniline
• 英文别名: N,N-dimethyl-3-phenylsulfanylaniline
• CAS: 103206-21-9
• 化学式: C₁₄H₁₅NS
• 分子量: 229.346
• InChiKey: SARWRHSYIKNWTM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  28.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-(二甲基氨基)苯硼酸 、 苯硫酚 在 copper diacetate 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 以80%的产率得到N,N-dimethyl-3-(phenylthio)aniline
  参考文献：
  名称：

  Copper Mediated Formation of Carbon-Heteroatom Bonds Using Organoboron Reagents and Ultrasound

  摘要：

  This report summarizes research efforts focused on copper acetate mediated reactions to form new carbon-heteroatom bonds using organoboron reagents under ultrasound irradiation. The method involves the application of ultrasound irradiation to the Chan-Evans-Lam reaction to achieve O-arylation of phenols, N-arylation of anilines and indoles, and S-arylation of thiols. Ultrasound irradiation was found to decrease reaction times from 72 hours to 4 hours while improving the product yields an average of 20%(1) Representative C-O, C-N, and C-S coupling reactions were successfully scaled-up from the milligram to gram levels while maintaining good product yields offering potential applications in industrial processes.

  DOI：

  10.3987/com-14-s(k)18

文献信息

• Palladium-Catalyzed Carbon−Sulfur Cross-Coupling Reactions with Indium Tri(organothiolate) and Its Application to Sequential One-Pot Processes
  作者：Jae-Young Lee、Phil Ho Lee

  DOI：10.1021/jo801169h

  日期：2008.9.19

  tri(organothiolate) is an effective nucleophilic coupling partner in Pd-catalyzed C-S cross-coupling reactions to produce the functionalized sulfides in excellent yields with high atom efficiency and complete regio- and chemoselectivity. The present method was efficiently applied to the sequential one-pot processes composed of selective double C-S cross-coupling reactions and addition of allylindium or allenylindium

  发现三（有机硫代铟）铟是钯催化的CS交叉偶联反应中有效的亲核偶联配偶体，以高产率，高原子效率和完全的区域选择性和化学选择性产生官能化的硫化物。本方法有效地应用于由选择性双CS交叉偶联反应和将烯丙基或烯丙基铟加入醛缩醛以形成官能化的硫化物和双（硫化物）组成的顺序一锅法。
• Cross-Coupling of Chloro(hetero)arenes with Thiolates Employing a Ni(0)-Precatalyst
  作者：Paul H. Gehrtz、Valentin Geiger、Tanno Schmidt、Laura Sršan、Ivana Fleischer

  DOI：10.1021/acs.orglett.8b03476

  日期：2019.1.4

  aryl chlorides and in situ generated aliphatic and aromatic thiolates is described. The employed on-cycle, air-stable defined Ni precatalysts allow for transformation of a broad scope of substrates. A variety of functional groups and heterocyclic motifs as well as structurally varied thiols are tolerated at unprecedented moderate catalyst loadings and reaction temperatures. Depending on reaction conditions

  描述了具有挑战性的芳基氯化物和原位生成的脂族和芳族硫醇盐的一般和高效的镍催化偶联。所使用的循环中，空气稳定的Ni定义型预催化剂可实现广泛范围的底物转化。在前所未有的中等催化剂负载量和反应温度下，可以耐受各种官能团和杂环基序以及结构上不同的硫醇。根据反应条件，芳基硫醇可以选择性地进行CS或CC偶联。
• 962. Search for spectral evidence of expansion of the valency shell of sulphur in aromatic sulphides
  作者：A. Mangini、R. Passerini

  DOI：10.1039/jr9560004954

  日期：——
• US4124370A
  申请人：——

  公开号：US4124370A

  公开（公告）日：1978-11-07