5,6,8-trifluoro-4-phenyl-3,4-dihydroquinolin-2-one | 1188002-08-5

• 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: 5,6,8-trifluoro-4-phenyl-3,4-dihydroquinolin-2-one
• 英文别名: 5,6,8-trifluoro-4-phenyl-3,4-dihydro-1H-quinolin-2-one
• CAS: 1188002-08-5
• 化学式: C₁₅H₁₀F₃NO
• 分子量: 277.246
• InChiKey: YOVGQDXFMACPEG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2,4,5-trifluoroanilide of cinnamic acid 在 三氟甲磺酸 作用下， 以42%的产率得到5,6,8-trifluoro-4-phenyl-3,4-dihydroquinolin-2-one
  参考文献：
  名称：

  Synthesis of polyfluorinated 4-phenyl-3,4-dihydroquinolin-2-ones and quinolin-2-ones via superacidic activation of N-(polyfluorophenyl)cinnamamides

  摘要：

  The cyclization reactions of a series of polyfluorocinnamanilides in triflic acid (CF3SO3H) yield 4-phenyl-3,4-dihydi-oquinolin-2-ones, which include a polyfluorinated benzene moiety as a part of the quinoline scaffold. These compounds undergo dehydrophenylation in the presence of AlCl3 to give the Corresponding polyfluoroquinolin-2-ones which are converted into polyfluorinated 2-chloroquinolines on treatment with POCl3. A mechanism for the cyclization reaction presuming the intermediacy of a superelectrophilic O,C-diprotonated form of the starting material is suggested. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.07.013