naphthalen-2-yl(2-(trifluoromethyl)phenyl)methanol | 906563-86-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: naphthalen-2-yl(2-(trifluoromethyl)phenyl)methanol
• 英文别名: Naphthalen-2-yl-[2-(trifluoromethyl)phenyl]methanol
• CAS: 906563-86-8
• 化学式: C₁₈H₁₃F₃O
• 分子量: 302.296
• InChiKey: ORDWZIQNWWXBCH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  邻溴三氟甲苯 在 potassium trimethylsilonate 、 四丁基氯化铵 、 仲丁基锂 作用下， 以 四氢呋喃 为溶剂， 反应 6.0h， 生成 naphthalen-2-yl(2-(trifluoromethyl)phenyl)methanol
  参考文献：
  名称：

  Bu₄N⁺ Alkoxide-Initiated/Autocatalytic Addition Reactions with Organotrimethylsilanes

  摘要：

  The use of Me3SiO(-)/Bu4N(+) as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.

  DOI：

  10.1021/jo5007637

文献信息

• Bu₄N⁺ Alkoxide-Initiated/Autocatalytic Addition Reactions with Organotrimethylsilanes
  作者：Manas Das、Donal F. O’Shea

  DOI：10.1021/jo5007637

  日期：2014.6.20

  The use of Me3SiO(-)/Bu4N(+) as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.