1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene | 269717-01-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene
• 英文别名: Methyl 3-[[4-[bis(3-methoxycarbonylazulen-1-yl)methyl]phenyl]-(3-methoxycarbonylazulen-1-yl)methyl]azulene-1-carboxylate
• CAS: 269717-01-3
• 化学式: C₅₆H₄₂O₈
• 分子量: 842.945
• InChiKey: RSGYZDODEADZSM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12
• 重原子数：
  64
• 可旋转键数：
  14
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  105
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene 在 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 氯仿 为溶剂， 反应 2.0h， 以45%的产率得到7,7,8,8-tetrakis(3-methoxycarbonyl-1-azulenyl)p-quinodimethane
  参考文献：
  名称：

  An efficient preparation and spectroscopic and electrochemical properties of quinodimethane derivatives with four 3-(methoxycarbonyl)azulen-1-yl groups

  摘要：

  Reaction of methyl 1-azuienecarboxylate (8) with terephthalaldehyde (9) in acetic acid in the presence of hydrochloric acid at 25 degrees C for 2 It gives 1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene (12), in 93% yield, which upon oxidation with 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) in dichloromethane in the presence of hexafluorophosphoric acid at 25 degrees C for I h affords the dicarbenium-ion compound 15 in 94% yield. Furthermore, reduction of 15 with zinc powder in a mixed solvent of acetonitrile and chloroform at 25 T for I h yields the target quinodi-methane 18 in 90% yield. Similarly, as in the case of 18, the quinoid compounds 19 and 20 can be derived from the dicarbenium-ion compounds 16 and 17, quantitatively. A facile preparation as well as spectroscopic and electrochemical properties of 15-20 is reported. (c) 2008 Elsevier Ltd. All fights reserved.

  DOI：

  10.1016/j.tet.2008.02.012
• 作为产物：
  描述：

  甲基1-薁羧酸酯 、 对苯二甲醛 在 盐酸 、 溶剂黄146 作用下， 反应 2.0h， 以93%的产率得到1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene
  参考文献：
  名称：

  An efficient preparation and spectroscopic and electrochemical properties of quinodimethane derivatives with four 3-(methoxycarbonyl)azulen-1-yl groups

  摘要：

  Reaction of methyl 1-azuienecarboxylate (8) with terephthalaldehyde (9) in acetic acid in the presence of hydrochloric acid at 25 degrees C for 2 It gives 1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene (12), in 93% yield, which upon oxidation with 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) in dichloromethane in the presence of hexafluorophosphoric acid at 25 degrees C for I h affords the dicarbenium-ion compound 15 in 94% yield. Furthermore, reduction of 15 with zinc powder in a mixed solvent of acetonitrile and chloroform at 25 T for I h yields the target quinodi-methane 18 in 90% yield. Similarly, as in the case of 18, the quinoid compounds 19 and 20 can be derived from the dicarbenium-ion compounds 16 and 17, quantitatively. A facile preparation as well as spectroscopic and electrochemical properties of 15-20 is reported. (c) 2008 Elsevier Ltd. All fights reserved.

  DOI：

  10.1016/j.tet.2008.02.012

文献信息

• An efficient preparation and spectroscopic and electrochemical properties of quinodimethane derivatives with four 3-(methoxycarbonyl)azulen-1-yl groups
  作者：Shin-ichi Takekuma、Kazutaka Sonoda、Toshie Minematsu、Hideko Takekuma

  DOI：10.1016/j.tet.2008.02.012

  日期：2008.4

  Reaction of methyl 1-azuienecarboxylate (8) with terephthalaldehyde (9) in acetic acid in the presence of hydrochloric acid at 25 degrees C for 2 It gives 1,4-bis[bis(3-methoxycarbonyl-1-azulenyl)methyl]benzene (12), in 93% yield, which upon oxidation with 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) in dichloromethane in the presence of hexafluorophosphoric acid at 25 degrees C for I h affords the dicarbenium-ion compound 15 in 94% yield. Furthermore, reduction of 15 with zinc powder in a mixed solvent of acetonitrile and chloroform at 25 T for I h yields the target quinodi-methane 18 in 90% yield. Similarly, as in the case of 18, the quinoid compounds 19 and 20 can be derived from the dicarbenium-ion compounds 16 and 17, quantitatively. A facile preparation as well as spectroscopic and electrochemical properties of 15-20 is reported. (c) 2008 Elsevier Ltd. All fights reserved.