Lithium N-(trifluoromethanesulfonyl)-2-(4-ethenylphenoxy)tetrafluoroethanesulfonamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: Lithium N-(trifluoromethanesulfonyl)-2-(4-ethenylphenoxy)tetrafluoroethanesulfonamide
• 英文别名: Lithium;[2-(4-ethenylphenoxy)-1,1,2,2-tetrafluoroethyl]sulfonyl-(trifluoromethylsulfonyl)azanide；lithium;[2-(4-ethenylphenoxy)-1,1,2,2-tetrafluoroethyl]sulfonyl-(trifluoromethylsulfonyl)azanide
• 化学式: C₁₁H₇F₇NO₅S₂*Li
• 分子量: 437.242
• InChiKey: CONNMCHVYKQLGM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.45
• 重原子数：
  27
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  95.3
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为产物：
  描述：

  乙烯 、 Lithium N-(trifluoromethanesulfonyl)-2-(4-bromophenoxy)tetrafluoroethanesulfonamide 在 palladium diacetate 三乙胺 、 三(邻甲基苯基)磷 作用下， 以 乙腈 为溶剂， 85.0 ℃ 、861.84 kPa 条件下， 反应 14.0h， 以81%的产率得到Lithium N-(trifluoromethanesulfonyl)-2-(4-ethenylphenoxy)tetrafluoroethanesulfonamide
  参考文献：
  名称：

  Aromatic monomers with pendant fluoroalkylsulfonate and sulfonimide groups

  摘要：

  Novel styrene and dimethylisophthalate monomers with pendant lithium fluoroalkylsulfonate or sulfonimide functional groups have been prepared from the corresponding phenolic intermediates. One route involves several steps and uses 1,2-dibromotetrafluoroethane as the key fluorinated intermediate. A second route with fewer steps utilizes a perfluoroalkylsulfonyl-substituted vinyl ether as the source of the fluorinated substituents but affords a product with significantly higher equivalent weight. (C) 2000 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0022-1139(00)00308-0

文献信息

• Aromatic monomers with pendant fluoroalkylsulfonate and sulfonimide groups
  作者：Andrew E. Feiring、Edward R. Wonchoba

  DOI：10.1016/s0022-1139(00)00308-0

  日期：2000.7

  Novel styrene and dimethylisophthalate monomers with pendant lithium fluoroalkylsulfonate or sulfonimide functional groups have been prepared from the corresponding phenolic intermediates. One route involves several steps and uses 1,2-dibromotetrafluoroethane as the key fluorinated intermediate. A second route with fewer steps utilizes a perfluoroalkylsulfonyl-substituted vinyl ether as the source of the fluorinated substituents but affords a product with significantly higher equivalent weight. (C) 2000 Elsevier Science S.A. All rights reserved.