[3-[[3-[[5-Benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-4-(2-methoxyethoxymethoxy)phenyl] benzoate | 192698-62-7

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 缩酚酸和缩酚酸环醚类
• 英文名称: [3-[[3-[[5-Benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-4-(2-methoxyethoxymethoxy)phenyl] benzoate
• CAS: 192698-62-7
• 化学式: C₁₃₉H₁₃₀O₂₃Si
• 分子量: 2196.63
• InChiKey: RQVBJYCMHZDGII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  27.15
• 重原子数：
  163
• 可旋转键数：
  57
• 环数：
  18.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  244
• 氢给体数：
  0
• 氢受体数：
  23

反应信息

• 作为反应物：
  描述：

  [3-[[3-[[5-Benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-4-(2-methoxyethoxymethoxy)phenyl] benzoate 在 4-甲基苯磺酸吡啶 作用下， 以 四氢呋喃 、 异丙醇 为溶剂， 生成 [3-[[3-[[5-Benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-4-hydroxyphenyl] benzoate
  参考文献：
  名称：

  Synthesis of Functionalized Aromatic Oligomers from a Versatile Diphenylmethane Template

  摘要：

  An efficient synthesis of the functionalized diphenylmethane system 1 is described. Selective unmasking of the latent phenol groups on 1 allowed the introduction of various appendages onto the diphenylmethane scaffold via simple alkylation, Mitsunobu etherification, and transition-metal-mediated C-C bond formation. Conversion of 1 to iodide 18 and benzylic zinc reagent 28 followed by palladium(0)-mediated coupling of these derivatives provided homologue 29. Repetitive application of this homologation protocol was used to prepare oligomers of chain length up to 16. Several examples of functional group manipulations on these higher order oligomers are presented. Diphenylmethane 1 was also employed as a key building block in the synthesis of the elastase inhibitor 67. The potential application of extended aromatic oligomers to the field of drug discovery is discussed.

  DOI：

  10.1021/jo970596h
• 作为产物：
  描述：

  benzoic acid 3-(5-(benzyloxy)-3-{5-(benzoyloxy)-3-[5-(benzyloxy)-3-(bromomethyl)-2-methoxybenzyl]-2-methoxybenzyl}-2-methoxybenzyl)-4-[(2-methoxyethoxy)methoxy]phenyl ester 在 四(三苯基膦)钯 、 1,2-二溴乙烷 、 锌 作用下， 以 四氢呋喃 为溶剂， 以70 g的产率得到[3-[[3-[[5-Benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[5-benzoyloxy-3-[[3-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-2-methoxyphenyl]methyl]-2-methoxy-5-phenylmethoxyphenyl]methyl]-4-(2-methoxyethoxymethoxy)phenyl] benzoate
  参考文献：
  名称：

  Synthesis of Functionalized Aromatic Oligomers from a Versatile Diphenylmethane Template

  摘要：

  An efficient synthesis of the functionalized diphenylmethane system 1 is described. Selective unmasking of the latent phenol groups on 1 allowed the introduction of various appendages onto the diphenylmethane scaffold via simple alkylation, Mitsunobu etherification, and transition-metal-mediated C-C bond formation. Conversion of 1 to iodide 18 and benzylic zinc reagent 28 followed by palladium(0)-mediated coupling of these derivatives provided homologue 29. Repetitive application of this homologation protocol was used to prepare oligomers of chain length up to 16. Several examples of functional group manipulations on these higher order oligomers are presented. Diphenylmethane 1 was also employed as a key building block in the synthesis of the elastase inhibitor 67. The potential application of extended aromatic oligomers to the field of drug discovery is discussed.

  DOI：

  10.1021/jo970596h

文献信息

• Synthesis of Functionalized Aromatic Oligomers from a Versatile Diphenylmethane Template
  作者：J. G. Bruno、M. N. Chang、Y. M. Choi-Sledeski、D. M. Green、D. G. McGarry、J. R. Regan、F. A. Volz

  DOI：10.1021/jo970596h

  日期：1997.7.1

  An efficient synthesis of the functionalized diphenylmethane system 1 is described. Selective unmasking of the latent phenol groups on 1 allowed the introduction of various appendages onto the diphenylmethane scaffold via simple alkylation, Mitsunobu etherification, and transition-metal-mediated C-C bond formation. Conversion of 1 to iodide 18 and benzylic zinc reagent 28 followed by palladium(0)-mediated coupling of these derivatives provided homologue 29. Repetitive application of this homologation protocol was used to prepare oligomers of chain length up to 16. Several examples of functional group manipulations on these higher order oligomers are presented. Diphenylmethane 1 was also employed as a key building block in the synthesis of the elastase inhibitor 67. The potential application of extended aromatic oligomers to the field of drug discovery is discussed.