2,2,3,3,4,4,5,5-octafluoro-N-(2,2,2-trifluoroethanethioyl)pentanamide | 1384866-37-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2,2,3,3,4,4,5,5-octafluoro-N-(2,2,2-trifluoroethanethioyl)pentanamide
• CAS: 1384866-37-8
• 化学式: C₇H₂F₁₁NOS
• 分子量: 357.147
• InChiKey: WATWTJUJSXFKJT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  61.2
• 氢给体数：
  1
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  2,2,3,3,4,4,5,5-octafluoro-N-(2,2,2-trifluoroethanethioyl)pentanamide 反应 40.0h， 生成 N,N'-[2,4-bis(trifluoromethyl)-1,3-dithietane-2,4-diyl]bis(2,2,3,3,4,4,5,5-octafluoropentanamide)
  参考文献：
  名称：

  Acylation of primary polyfluoroalkanethioamides

  摘要：

  The reaction conditions and the nature of acyl chloride strongly influence the outcome of the primary polyfluoroalkanethioamides acylation. Preparation of NH-acetyl polyfluoroalkanethioamides was achieved conducting the reactions in acetonitrile at -20 degrees C in the presence of pyridine. The reactions of polyfluoroalkanethioamides with 5-hydroperfluoropentanoyl chloride are efficient for the synthesis of NH-acyl derivatives when they were carried out in the absence of a base under heating at 100 degrees C. The obtained NH-acyl polyfluoroalkanethioamides enter into cycloaddition reactions with 2,3-dimethylbutadiene at room temperature. (C) 2012 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jfluchem.2012.05.008
• 作为产物：
  描述：

  5H-八氟氯戊醇 、 2,2,2-三氟乙烷硫代酰胺 反应 1.0h， 以84%的产率得到2,2,3,3,4,4,5,5-octafluoro-N-(2,2,2-trifluoroethanethioyl)pentanamide
  参考文献：
  名称：

  Acylation of primary polyfluoroalkanethioamides

  摘要：

  The reaction conditions and the nature of acyl chloride strongly influence the outcome of the primary polyfluoroalkanethioamides acylation. Preparation of NH-acetyl polyfluoroalkanethioamides was achieved conducting the reactions in acetonitrile at -20 degrees C in the presence of pyridine. The reactions of polyfluoroalkanethioamides with 5-hydroperfluoropentanoyl chloride are efficient for the synthesis of NH-acyl derivatives when they were carried out in the absence of a base under heating at 100 degrees C. The obtained NH-acyl polyfluoroalkanethioamides enter into cycloaddition reactions with 2,3-dimethylbutadiene at room temperature. (C) 2012 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jfluchem.2012.05.008