1,4-Diphenyl-2-(trifluoromethyl)-1,2-dihydroquinoline | 128644-90-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 1,4-Diphenyl-2-(trifluoromethyl)-1,2-dihydroquinoline
• 英文别名: 1,4-diphenyl-2-(trifluoromethyl)-2H-quinoline
• CAS: 128644-90-6
• 化学式: C₂₂H₁₆F₃N
• 分子量: 351.371
• InChiKey: ATJRGCWBZLYDQU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  26
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  3.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  N,N-Diphenyl-N-(2,2,2-trifluoroethyl)amine 在 氢氧化钾 、 四氯化钛 作用下， 以 二氯甲烷 为溶剂， 生成 1,4-Diphenyl-2-(trifluoromethyl)-1,2-dihydroquinoline
  参考文献：
  名称：

  Cationic Polar Cycloaddition with Anodically Prepared a-Tri- and a-Difluoromethylated N,O-Acetals: Preparation of Fluoromethylated Tetra- and Dihydroquinoline Derivatives

  摘要：

  DOI：

  10.3987/com-89-5295

文献信息

• Cationic Polar Cycloaddition with Anodically Prepared a-Tri- and a-Difluoromethylated N,O-Acetals: Preparation of Fluoromethylated Tetra- and Dihydroquinoline Derivatives
  作者：Toshio Fuchigami、Shinji Ichikawa、Zaghloul e. Kandeel、Akinori Konno、Tsutomu Nonaka

  DOI：10.3987/com-89-5295

  日期：——
• FUCHIGAMI, TOSHIO;ICHIKAWA, SHINJI;KANDEEL, ZAGHLOUL E.;KONNO, AKINORI;NO+, HETEROCYCLES, 31,(1990) N, C. 415-417
  作者：FUCHIGAMI, TOSHIO、ICHIKAWA, SHINJI、KANDEEL, ZAGHLOUL E.、KONNO, AKINORI、NO+

  DOI：——

  日期：——
• Electrolytic Reactions of Fluoroorganic Compounds. 14. Regioselective Anodic Methoxylation of N-(Fluoroethyl)amines. Preparation of Highly Useful Fluoroalkylated Building Blocks
  作者：Toshio Fuchigami、Shinji Ichikawa

  DOI：10.1021/jo00082a018

  日期：1994.2

  Anodic methoxylation of various types of N-(fluoroethyl)amines, ArRNCH(2)R(f) (R(f) = CF3, CHF2, CH2F, etc.) has been systematically studied and it was found that a methoxy group was exclusively or preferentially introduced into the position a to the fluoromethyl (R(f)) group, depending on the R(f) and R groups. The effect of the R(f) group on the promotion of the anodic alpha-methoxylation decreased in the order CF3, CHF2, and CH2F. This remarkable promotion effect and unique regioselectivity can be explained mainly in terms of the alpha-CH kinetic acidities of the cation radicals formed by one-electron oxidation of the amines. The alpha-methoxylated products are highly useful precursors for the construction of carbon-carbon bonds alpha to the trifluoromethyl and difluoromethyl groups, which is difficult by other methods.