2'-phenylspiro[cyclohexane-1,1'-isoindolin]-3'-one | 23659-75-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 2'-phenylspiro[cyclohexane-1,1'-isoindolin]-3'-one
• 英文别名: Spiro<2-phenyl-phthalimidin-3,1'-cyclohexan>；2'-Phenylspiro[cyclohexane-1,3'-isoindole]-1'-one
• CAS: 23659-75-8
• 化学式: C₁₉H₁₉NO
• 分子量: 277.366
• InChiKey: XTLVEWPHCZLSCF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-环己基苯甲酸 在 草酰氯 、 2-碘联苯 、 potassium carbonate 、 N,N-二甲基甲酰胺 、 间氯过氧苯甲酸 作用下， 以 二氯甲烷 、 水 、 乙酸乙酯 为溶剂， 反应 72.0h， 生成 2'-phenylspiro[cyclohexane-1,1'-isoindolin]-3'-one
  参考文献：
  名称：

  Iodoarene-Catalyzed Stereospecific Intramolecular sp³ C–H Amination: Reaction Development and Mechanistic Insights

  摘要：

  A new strategy is reported for intramolecular Sp(3) C-H amination :under mild reaction conditions using iodoarene as catalyst and m-CPBA as oxidant. This C-H functionalization involving iodine(III) reagents generated in situ occurs readily at sterically hindered tertiary C-H bonds. DFT (M06-2X) calculations show that the preferred pathway involves an iodonium cation intermediate and proceeds via an energetically concerted transition state, through hydride transfer followed by the spontaneous C-N bond formation. ThiS leads to the experimentally observed amination at a chiral center without loss of stereo chemical information.

  DOI：

  10.1021/jacs.5b03488

文献信息

• Iodoarene-Catalyzed Stereospecific Intramolecular sp³ C–H Amination: Reaction Development and Mechanistic Insights
  作者：Chendan Zhu、Yong Liang、Xin Hong、Heqing Sun、Wei-Yin Sun、K. N. Houk、Zhuangzhi Shi

  DOI：10.1021/jacs.5b03488

  日期：2015.6.24

  A new strategy is reported for intramolecular Sp(3) C-H amination :under mild reaction conditions using iodoarene as catalyst and m-CPBA as oxidant. This C-H functionalization involving iodine(III) reagents generated in situ occurs readily at sterically hindered tertiary C-H bonds. DFT (M06-2X) calculations show that the preferred pathway involves an iodonium cation intermediate and proceeds via an energetically concerted transition state, through hydride transfer followed by the spontaneous C-N bond formation. ThiS leads to the experimentally observed amination at a chiral center without loss of stereo chemical information.