4,5-dimethyl ethyl 2-cyanobenzoate

• 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: 4,5-dimethyl ethyl 2-cyanobenzoate
• 英文别名: Ethyl 2-cyano-4,5-dimethylbenzoate；ethyl 2-cyano-4,5-dimethylbenzoate
• 化学式: C₁₂H₁₃NO₂
• 分子量: 203.241
• InChiKey: CCMLMJZXVPCZSG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  50.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  N-[3-cyano-3-ethoxy-5,6-dimethyl-1(3H)-isobenzofuranylidene]-2-methyl-2-propanamine 在 三(五氟苯基)硼烷 作用下， 以 四氢呋喃 为溶剂， 反应 8.0h， 以89%的产率得到4,5-dimethyl ethyl 2-cyanobenzoate
  参考文献：
  名称：

  Skeletal Rearrangement of Cyano-Substituted Iminoisobenzofurans into Alkyl 2-Cyanobenzoates Catalyzed by B(C₆F₅)₃

  摘要：

  An efficient method for the direct conversion of cyano-substituted iminoisobenzofurans into their corresponding alkyl 2-cyanobenzoates has been developed. This transformation proceeds via cleavage of C-C, C-O, and C-N bonds in starting iminoisobenzofurans. DFT study revealed that intermediate a-iminonitriles are produced in situ via C-C bond formation between 2-iminium benzoates and a cyanide ion. Generation of isocyanide as the byproduct in a more thermodynamic manner in DFT calculations also supports the experimental results.

  DOI：

  10.1021/ol5026519

文献信息

• Skeletal Rearrangement of Cyano-Substituted Iminoisobenzofurans into Alkyl 2-Cyanobenzoates Catalyzed by B(C₆F₅)₃
  作者：Jing Li、Yasuhiro Okuda、Jiaji Zhao、Seiji Mori、Yasushi Nishihara

  DOI：10.1021/ol5026519

  日期：2014.10.3

  An efficient method for the direct conversion of cyano-substituted iminoisobenzofurans into their corresponding alkyl 2-cyanobenzoates has been developed. This transformation proceeds via cleavage of C-C, C-O, and C-N bonds in starting iminoisobenzofurans. DFT study revealed that intermediate a-iminonitriles are produced in situ via C-C bond formation between 2-iminium benzoates and a cyanide ion. Generation of isocyanide as the byproduct in a more thermodynamic manner in DFT calculations also supports the experimental results.