2-((4-phenylbutan-2-yl)thio)benzo[d]thiazole | 820961-86-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 2-((4-phenylbutan-2-yl)thio)benzo[d]thiazole
• 英文别名: 2-(1-methyl-3-phenylpropylsulfanyl)-1,3-benzothiazole；2-[(4-Phenylbutan-2-yl)sulfanyl]-1,3-benzothiazole；2-(4-phenylbutan-2-ylsulfanyl)-1,3-benzothiazole
• CAS: 820961-86-2
• 化学式: C₁₇H₁₇NS₂
• 分子量: 299.461
• InChiKey: IPSINPVEATXCAA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  66.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-((4-phenylbutan-2-yl)thio)benzo[d]thiazole 在 hexaammonium heptamolybdate tetrahydrate 、 双氧水 作用下， 以 乙醇 、 水 为溶剂， 生成
  参考文献：
  名称：

  金属自由基介导的乙烯和低沸点烯烃的烷基官能化

  摘要：

  烯烃，特别是乙烯等低沸点烯烃，是石油化工中的大宗化工原料。将这些廉价材料转化为增值的精细化学品至关重要。在此，我们报告了一种通过远程官能团迁移对气态乙烯和其他轻质烯烃进行自由基烷基官能化的有效方法。随着额外的杂芳基或肟基的安装，包括氘代烷基在内的各种烷基很容易并入烯烃中，从而产生复杂的官能化烷烃。这种光化学方法操作简单，即使在没有光敏剂和过渡金属添加剂的情况下也能进行。

  DOI：

  10.1039/d3gc01040f
• 作为产物：
  描述：

  4-苯基-2-丁醇 在 樟脑醌 、 三乙胺 作用下， 以 氘代氯仿 、 氯仿 为溶剂， 反应 14.0h， 生成 2-((4-phenylbutan-2-yl)thio)benzo[d]thiazole
  参考文献：
  名称：

  Camphorquinone: a new and efficient oxidant for the preparation of 2-thio-substituted benzothiazoles from alcohols by oxidation-reduction condensation

  摘要：

  A convenient one-pot procedure for the preparation of various 2-thio-substituted benzothiazoles from alcohols and benzothiazole-2-thiol utilizing camphorquinone-mediated oxidation-reduction condensation is disclosed. The condensation between benzothiazole-2-thiol and alkyl diphenylphosphinites, generated in situ from alcohols and chlorodiphenylphosphine, proceeded smoothly in the presence of camphorquinone to furnish the corresponding benzothiazoles in good to moderate yields.[GRAPHICS].

  DOI：

  10.1080/17415993.2014.907408

文献信息

• Conversion of Alcohols to Alkyl Aryl Sulfides by a New Type of Oxidation–Reduction Condensation Using Phenyl Diphenylphosphinite
  作者：Kiichi Kuroda、Yuji Maruyama、Yujiro Hayashi、Teruaki Mukaiyama

  DOI：10.1246/bcsj.82.381

  日期：2009.3.15

  Preparation of alkyl aryl sulfides from alcohols and arenethiols such as 2-sulfanyl-1,3-benzothiazole (BtzSH) is described by a new type of oxidation–reduction condensation using phenyl diphenylpho...

  从醇和芳烃硫醇如 2-硫烷基-1,3-苯并噻唑 (BtzSH) 制备烷基芳基硫化物是通过使用苯基二苯基膦的一种新型氧化还原缩合反应来描述的。
• Preparation of Alkyl Aryl Sulfides from Alcohols and 2-Sulfanylbenzothiazole by a New Type of Oxidation–Reduction Condensation Using Aryl Diphenylphosphinite and Benzoquinone Derivatives
  作者：Kiichi Kuroda、Yujiro Hayashi、Teruaki Mukaiyama

  DOI：10.1246/cl.2008.592

  日期：2008.6.5

  A method for the preparation of alkyl aryl sulfides from alcohols and 2-sulfanylbenzothiazole by a new type of oxidation–reduction condensation using phenyl diphenylphosphinite and 2,6-dimethoxy-1,...

  一种使用苯基二苯基亚膦酸酯和 2,6-二甲氧基-1, 以新型氧化还原缩合反应由醇和 2-硫烷基苯并噻唑制备烷基芳基硫化物的方法
• A New Method for the Preparation of Alkyl Aryl Sulfides from Alcohols via Alkoxydiphenylphosphines by Oxidation–Reduction Condensation
  作者：Teruaki Mukaiyama、Kazuhiro Ikegai

  DOI：10.1246/cl.2004.1522

  日期：2004.11

  A new method for the preparation of alkyl aryl sulfides from alcohols via alkoxydiphenylphosphines by oxidation-reduction condensation was established. Various primary, secondary, and tertiary alcohols were successfully converted into the corresponding sulfides in moderate to high yields.

  建立了烷氧基二苯基膦氧化还原缩合醇合成烷基芳基硫化物的新方法。各种伯醇、仲醇和叔醇以中等至高产率成功转化为相应的硫化物。
• Stereospecific Synthesis of Alkyl Aryl Sulfides from Alcohols and 2-Sulfanylbenzothiazole Using Aryl Diphenylphosphinite and Azide Compounds by a New Type of Oxidation–Reduction Condensation
  作者：Kiichi Kuroda、Yuji Maruyama、Yujiro Hayashi、Teruaki Mukaiyama

  DOI：10.1246/cl.2008.836

  日期：2008.8.5

  The preparation of alkyl aryl sulfides from alcohols and 2-sulfanylbenzothiazole using phenyl diphenylphosphinite and azide compounds by a new type of oxidation–reduction condensation is described....

  描述了使用苯基二苯基次膦酸盐和叠氮化合物通过新型氧化还原缩合反应从醇和 2-硫烷基苯并噻唑制备烷基芳基硫化物。
• A New Type of Oxidation-Reduction Condensation by the Combined Use of Phenyl Diphenylphosphinite and Oxidant
  作者：Teruaki Mukaiyama、Kiichi Kuroda、Yuji Maruyama

  DOI：10.3987/rev-09-sr(s)1

  日期：——

  A new type of oxidation-reduction condensation of alcohols with sulfur, nitrogen, and oxygen nucleophiles by the combined use of phenyl diphenylphosphinite (PhOPPh2) and oxidants such as azides or diethyl azodicarboxylate (DEAD) are described. In these reactions, chiral secondary and tertiary alcohols are converted into the corresponding chiral sulfides, azides, esters and ethers under mild and neutral conditions with almost complete inversion of stereochemical configuration.