butane 1,4-di-(2-methoxycarbonyloxy)cinnamate | 252258-25-6

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: butane 1,4-di-(2-methoxycarbonyloxy)cinnamate
• CAS: 252258-25-6
• 化学式: C₂₆H₂₆O₁₀
• 分子量: 498.486
• InChiKey: DNZPLMNUCYBJSF-WXUKJITCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.57
• 重原子数：
  36.0
• 可旋转键数：
  11.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  123.66
• 氢给体数：
  0.0
• 氢受体数：
  10.0

反应信息

• 作为反应物：
  描述：

  butane 1,4-di-(2-methoxycarbonyloxy)cinnamate 在 ammonium hydroxide 作用下， 以 乙醇 为溶剂， 反应 16.0h， 以89%的产率得到butane 1,4-di-(2-hydroxy)cinnamate
  参考文献：
  名称：

  Effect of Substitution on the 2+2 Cycloaddition Reaction of Phenylpropanoids

  摘要：

  Formation of the cyclobutane products truxillic and truxinic acid within the plant cell wall could occur by photocycloaddition or possibly by enzyme-mediated radical coupling. Model precursors were synthesized and the mode of formation of the cyclobutane products was investigated. Modeling studies suggested that all the model compounds with the exception of the 2-hydroxylated diester contained the correct geometry for photocyclization and this was confirmed by irradiation. Delocalization of the unpaired electron was measured by ESR and the photochemical reaction rates were compared with the partial atomic orbital population of the singly occupied molecular orbital. It was observed that the 3-hydroxylated derivative had almost no delocalization to C8 and the lowest reaction rate. The rate of reaction increased with increasing extent of methoxylation. Incubation with silver oxide or with peroxidase failed to induce intramolecular dimerization. These results suggest that the biological mode of formation of truxillic and truxinic acid is the most likely via light-catalyzed 2+2 cycloaddition. (C) 1999 Academic Press.

  DOI：

  10.1006/bioo.1999.1143
• 作为产物：
  描述：

  反式-2-羟基肉桂酸 在 吡啶 、 sodium hydroxide 、 氯化亚砜 作用下， 以 甲苯 为溶剂， 反应 29.5h， 生成 butane 1,4-di-(2-methoxycarbonyloxy)cinnamate
  参考文献：
  名称：

  Effect of Substitution on the 2+2 Cycloaddition Reaction of Phenylpropanoids

  摘要：

  Formation of the cyclobutane products truxillic and truxinic acid within the plant cell wall could occur by photocycloaddition or possibly by enzyme-mediated radical coupling. Model precursors were synthesized and the mode of formation of the cyclobutane products was investigated. Modeling studies suggested that all the model compounds with the exception of the 2-hydroxylated diester contained the correct geometry for photocyclization and this was confirmed by irradiation. Delocalization of the unpaired electron was measured by ESR and the photochemical reaction rates were compared with the partial atomic orbital population of the singly occupied molecular orbital. It was observed that the 3-hydroxylated derivative had almost no delocalization to C8 and the lowest reaction rate. The rate of reaction increased with increasing extent of methoxylation. Incubation with silver oxide or with peroxidase failed to induce intramolecular dimerization. These results suggest that the biological mode of formation of truxillic and truxinic acid is the most likely via light-catalyzed 2+2 cycloaddition. (C) 1999 Academic Press.

  DOI：

  10.1006/bioo.1999.1143