1-[diisopropyl(pyrimidin-2-yl)silyl]-2-naphthyl pivalate | 1369625-87-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1-[diisopropyl(pyrimidin-2-yl)silyl]-2-naphthyl pivalate
• CAS: 1369625-87-5
• 化学式: C₂₅H₃₂N₂O₂Si
• 分子量: 420.627
• InChiKey: CJNGOEBAWFRYGC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.96
• 重原子数：
  30.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  52.08
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  2-(diisopropylsilyl)pyrimidine 在 dirhodium tetraacetate 、 potassium phosphate 、 lithium acetate 、 palladium diacetate 作用下， 以 1,4-二氧六环 、 1,2-二氯乙烷 为溶剂， 反应 40.0h， 生成 1-[diisopropyl(pyrimidin-2-yl)silyl]-2-naphthyl pivalate
  参考文献：
  名称：

  Double-Fold C–H Oxygenation of Arenes Using PyrDipSi: a General and Efficient Traceless/Modifiable Silicon-Tethered Directing Group

  摘要：

  The efficient Pd-catalyzed double-fold C-H oxygenation of arenes into resorcinols using the newly developed 2-pyrimidyldiisopropylsilyl (PyrDipSi) directing group is described. Its use allows for the sequential introduction of OAc and OPiv groups in a one-pot manner to produce orthogonally protected resorcinol derivatives. The PyrDipSi group is superior to the previously developed 2-pyridyldiisopropylsilyl (PyDipSi) group, as it is efficient for monooxygenation of ortho-substituted arenes. Notably, the PyrDipSi group can be easily installed into arene molecules and can be easily removed or modified after the oxygenation reaction.

  DOI：

  10.1021/ja3010545