1-chloro-3-(4-chlorophenylsulfanyl)propan-2-ol | 2989-38-0

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 1-chloro-3-(4-chlorophenylsulfanyl)propan-2-ol
• 英文别名: 1-chloro-3-((4-chlorophenyl)thio)propan-2-ol；1-chloro-3-(4-chlorophenylthio)propan-2-ol；gwx-911；1-chloro-3-(4-chloro-phenylsulfanyl)-propan-2-ol；1-Chlor-3-(4-chlor-phenylmercapto)-propan-2-ol；p-Chlorphenyl-γ-Cl-β-OH-propylsulfid；1-Chloro-3-[(4-chlorophenyl)sulfanyl]propan-2-ol；1-chloro-3-(4-chlorophenyl)sulfanylpropan-2-ol
• CAS: 2989-38-0
• 化学式: C₉H₁₀Cl₂OS
• 分子量: 237.15
• InChiKey: ZAWGYCFTGIBCCJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  45.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  乙酸乙烯酯 、 1-chloro-3-(4-chlorophenylsulfanyl)propan-2-ol 在 Novozyme SP 435 Candida antarctica lipase 作用下， 以 甲苯 为溶剂， 反应 45.0h， 生成 (S)-1-chloro-3-((4-chlorophenyl)thio)propan-2-ol 、 (R)-1-chloro-3-((4-chlorophenyl)thio)propan-2-ol 、 (R)-(-)-1-chloro-3-((4-chlorophenyl)thio)propan-2-yl acetate 、 (S)-(-)-1-chloro-3-((4-chlorophenyl)thio)propan-2-yl acetate
  参考文献：
  名称：

  Lipase-catalyzed separation of the enantiomers of 1-substituted-3-arylthio-2-propanols

  摘要：

  Optically active (R)- and (S)-1-substituted-3-(arylthio)propan-2-ols have been prepared in the reaction of the appropriate 2-(arylthiomethyl)oxiranes with chloride and azide anions followed by a lipase-catalyzed transesterification. The effects of the enzyme preparation as well as of the reaction conditions have been compared in terms of the enantiomeric excess of the obtained acetate and unreacted alcohol. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.01.040
• 作为产物：
  描述：

  (4-chloro-phenylsulfanylmethyl)-oxirane 在 potassium chloride 、 氯化铵 作用下， 以 甲醇 、 水 为溶剂， 生成 1-chloro-3-(4-chlorophenylsulfanyl)propan-2-ol
  参考文献：
  名称：

  Lipase-catalyzed separation of the enantiomers of 1-substituted-3-arylthio-2-propanols

  摘要：

  Optically active (R)- and (S)-1-substituted-3-(arylthio)propan-2-ols have been prepared in the reaction of the appropriate 2-(arylthiomethyl)oxiranes with chloride and azide anions followed by a lipase-catalyzed transesterification. The effects of the enzyme preparation as well as of the reaction conditions have been compared in terms of the enantiomeric excess of the obtained acetate and unreacted alcohol. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.01.040

文献信息

• Facile Room-Temperature MgBr₂· OEt₂-Catalyzed Thiolysis of Epoxides Under Solvent-Free Conditions
  作者：Mohammad M. Mojtahedi、M. Saeed Abaee、Mohammad Bolourtchian、Hassan Abbasi

  DOI：10.1080/10426500601088697

  日期：2007.2.15

  Solvent-free ring opening of 1,2-epoxides with aromatic and aliphatic thiols under 1 mol% magnesium bromide ethyl etherate catalysis affords rapid formation of β-hydroxy sulfides at ambient temperature with excellent yields. Nucleophilic attack of the thiols occurs regioselectively at the less hindered position of the epoxides.

  在 1 mol% 溴化镁乙基醚合物催化下，1,2-环氧化物与芳香族和脂肪族硫醇的无溶剂开环可在环境温度下以优异的产率快速形成 β-羟基硫化物。硫醇的亲核攻击区域选择性地发生在环氧化物的受阻较小的位置。
• Alumina-supported Molybdenum (VI) Oxide: An Efficient and Recyclable Heterogeneous Catalyst for Regioselective Ring Opening of Epoxides with Thiols, Acetic Anhydride, and Alcohols under Solvent-free Conditions
  作者：Sweety Singhal、Suman L. Jain、Bir Sain

  DOI：10.1246/cl.2008.620

  日期：2008.6.5

  An efficient and simple protocol for regioselective ring opening of epoxides with thiols, acetic anhydride, and alcohols using 16 wt % MoO3 supported on alumina as a recyclable catalyst is described.

  描述了使用负载在氧化铝上的 16 wt% MoO3 作为可回收催化剂的硫醇、乙酸酐和醇区域选择性开环环氧化物的有效且简单的方案。
• Efficient Synthesis of <font>β</font>-Hydroxy Sulfides and <font>β</font>-Hydroxy Sulfoxides Catalyzed by Cu/MgO Under Solvent-Free Conditions
  作者：Biswanath Das、Penagaluri Balasubramanyam、Maddeboina Krishnaiah、Boyapati Veeranjaneyulu、Dega Sudhakar

  DOI：10.1080/00397910903219500

  日期：2010.6.25

  Regio-, stereo-, and chemoselective ring opening of epoxides with thiols using Cu/MgO as a heterogeneous catalyst has efficiently been carried out to produce the corresponding β-hydroxy sulfides in excellent yields at room temperature under solvent-free conditions. The treatment of the epoxides with thiols and 50% aqueous H2O2 in the presence of the same catalyst at room temperature affords the β-hydroxy

  使用 Cu/MgO 作为多相催化剂，环氧化物与硫醇的区域选择性、立体选择性和化学选择性开环已被有效地进行，以在室温和无溶剂条件下以优异的产率生产相应的 β-羟基硫化物。在室温下，在相同催化剂的存在下，用硫醇和 50% 的 H2O2 水溶液处理环氧化物以极好的收率提供了 β-羟基亚砜。
• SOME ARALKYL AND ARYL ALKYL SULPHIDES AND DISULPHIDES
  作者：Marshall Kulka、F. G. Van Stryk

  DOI：10.1139/v57-073

  日期：1957.6.1

  Sixty sulphides and disulphides have been prepared from mercaptans and alkyl and alkylene halides for testing as insecticides.

  已经从硫醇和烷基卤化物和亚烷基卤化物制备了 60 种硫化物和二硫化物，用于作为杀虫剂进行测试。
• Complex catalyst, process for producing the complex catalyst, and process for producing alchohol derivative with the complex catalyst
  申请人：——

  公开号：US20040077487A1

  公开（公告）日：2004-04-22

  There are provided (asymmetric) complex catalysts comprising metal complexes and Lewis acids as components, the metal complex being of formula (1): 1 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and are independently hydrogen, halogen, alkyl or the like; one of R 9 and R 10 is hydrogen and the other is alkyl of 1 to 4 carbon atoms or the like; Q is a single bond or alkylene of 1 to 4 carbon atoms; M is a metal ion; and A is a balancing counter ion or ligand; processes for the production of these complex catalysts; processes for the production of (optically active) alcohol derivatives, characterized in that cyclic ether compounds are reacted with phenol derivatives in the presence of these complex catalysts; and further processes for producing (optically active) nitrogen-containing heterocyclic compounds by reacting these alcohol derivatives with halogenated nitrogen-containing heterocyclic compounds in the presence of a base.

  提供了由金属配合物和路易斯酸组成的（不对称的）复杂催化剂，其中金属配合物的化学式为（1）：1其中R1、R2、R3、R4、R5、R6、R7和R8相同或不同，独立地是氢、卤素、烷基或类似物；R9和R10中的一个是氢，另一个是1至4个碳原子的烷基或类似物；Q是单键或1至4个碳原子的烷基；M是金属离子；A是平衡的反离子或配体；制备这些复杂催化剂的方法；制备（光学活性的）醇衍生物的方法，其特征在于在这些复杂催化剂的存在下，环氧化合物与酚衍生物反应；以及在碱的存在下，通过将这些醇衍生物与卤素化的含氮杂环化合物反应，制备（光学活性的）含氮杂环化合物的进一步方法。