(2-methyl-1-phenylprop-2-yl)(phenyl)sulfane | 79399-22-7

• 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: (2-methyl-1-phenylprop-2-yl)(phenyl)sulfane
• 英文别名: phenyl (2-methyl-1-phenyl)but-2-yl sulphide；Benzene, [(1,1-dimethyl-2-phenylethyl)thio]-；(2-methyl-1-phenylpropan-2-yl)sulfanylbenzene
• CAS: 79399-22-7
• 化学式: C₁₆H₁₈S
• 分子量: 242.385
• InChiKey: DTQJBHPHIZDPGG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (2-methyl-1-phenylprop-2-yl)(phenyl)sulfane 在 尿素 作用下， 生成 1,1-dimethyl-2-phenylethyl phenyl sulfoxide
  参考文献：
  名称：

  Photolysis of Alkyl Aryl Sulfoxides:  α-Cleavage, Hydrogen Abstraction, and Racemization¹

  摘要：

  The photochemistry of a series of alkyl aryl sulfoxides is described. The initial event of the photolysis process is homolytic cleavage to form sulfinyl/alkyl radical pairs. The radical pair partitions between recombination to starting material, formation of sulfenic esters, disproportionation to an olefin and benzenesulfenic acid, and formation of typical radical escape products. The quantum yield for conversion depends on the structure or the reactivity of the alkyl radical, with the sequence benzyl > tertiary alkyl > secondary alkyl > primary alkyl > (di)aryl. The high racemization efficiency of some aryl primary-alkyl sulfoxides suggests that another nonradical pathway for the photoracemization process may exist. Product analysis does not support any hydrogen abstraction pathways.

  DOI：

  10.1021/jo961775m
• 作为产物：
  描述：

  二甲基苄基原醇 在 tris(pentafluorophenyl)borane hydrate 、 二乙胺基三氟化硫 作用下， 以 硝基甲烷 、 二氯甲烷 为溶剂， 反应 1.0h， 生成 (2-methyl-1-phenylprop-2-yl)(phenyl)sulfane
  参考文献：
  名称：

  催化脂肪族氟化物B（C 6 F 5）3 H 2 O促进的脱氟官能化

  摘要：

  描述了在良性反应条件下进行的AB（C 6 F 5）3 H 2 O催化的叔脂肪族氟化物的脱氟官能化。通过快速有效地形成一系列具有新安装的C（sp 3）N，S，C和O键的产品，可以举例说明该方法的综合用途。这项研究说明了其他惰性原料的广泛反应性，并提供了通往有价值的和合成上代表性不足的产品的途径，这些产品以前从未从此类氟化前体中获得。

  DOI：

  10.1016/j.jfluchem.2016.11.005

文献信息

• A Novel Synthesis oftert- Alkyl Sulfides
  作者：Alan R. Katritzky、Subbu Perumal、Wojciech Kuzmierkiewicz、Ping Lue、John V. Greenhill

  DOI：10.1002/hlca.19910740829

  日期：1991.12.11

  tert- Alkyl sulfides are conveniently prepared from α-(1H-benzotriazol-1-yl)alkyl sulfides by displacement of the 1H-benzotriazol-1-yl group with Grignard reagents. The 1-[α-(alkylthio)alkyl]- and 1-[α-(arylthio)alkyl]-1H-benzotriazole intermediates are easily available by several routes: (i) displacement of the halogen from appropriate halides by sodium salts of thiols, (ii) condensation of 1H-benzotriazole

  叔烷基硫醚可通过用格氏试剂置换1 H-苯并三唑-1-基，由α-（1 H-苯并三唑-1-基）烷基硫化物方便地制备。1- [α-（烷硫基）烷基] -和1- [α-（芳硫基）烷基] -1 ħ苯并三唑的中间体很容易获得由几个路线：（我）通过的钠盐从适当卤化物置换卤素硫醇，（ii）1 H-苯并三唑和硫醇与羰基化合物的缩合，或（iii）N-取代的1 H-苯并三唑的锂化，随后用亲电试剂处理。
• A biomimetic synthesis of chrysanthemol
  作者：D. Babin、J.D. Fourneron、L.M. Harwood、M. Julia

  DOI：10.1016/s0040-4020(01)92018-6

  日期：1981.1
• Catalytic B(C6F5)3H2O-promoted defluorinative functionalization of tertiary aliphatic fluorides
  作者：Marian Dryzhakov、Edward Richmond、Guang Li、Joseph Moran

  DOI：10.1016/j.jfluchem.2016.11.005

  日期：2017.1

  A B(C6F5)3H2O-catalyzed defluorinative functionalization of tertiary aliphatic fluorides is described that proceeds under benign reaction conditions. The synthetic utility of the method is exemplified through the fast and efficient formation of a range of products with newly installed C(sp3) N, S, C and O bonds. This study illustrates the broad reactivity of otherwise inert starting materials and provides

  描述了在良性反应条件下进行的AB（C 6 F 5）3 H 2 O催化的叔脂肪族氟化物的脱氟官能化。通过快速有效地形成一系列具有新安装的C（sp 3）N，S，C和O键的产品，可以举例说明该方法的综合用途。这项研究说明了其他惰性原料的广泛反应性，并提供了通往有价值的和合成上代表性不足的产品的途径，这些产品以前从未从此类氟化前体中获得。
• Photolysis of Alkyl Aryl Sulfoxides:  α-Cleavage, Hydrogen Abstraction, and Racemization¹
  作者：Yushen Guo、William S. Jenks

  DOI：10.1021/jo961775m

  日期：1997.2.1

  The photochemistry of a series of alkyl aryl sulfoxides is described. The initial event of the photolysis process is homolytic cleavage to form sulfinyl/alkyl radical pairs. The radical pair partitions between recombination to starting material, formation of sulfenic esters, disproportionation to an olefin and benzenesulfenic acid, and formation of typical radical escape products. The quantum yield for conversion depends on the structure or the reactivity of the alkyl radical, with the sequence benzyl > tertiary alkyl > secondary alkyl > primary alkyl > (di)aryl. The high racemization efficiency of some aryl primary-alkyl sulfoxides suggests that another nonradical pathway for the photoracemization process may exist. Product analysis does not support any hydrogen abstraction pathways.