3-[2-(3-Aminomethyl-2-methyl-phenyl)-acenaphthylen-1-yl]-2-methyl-benzylamine | 127158-74-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: 3-[2-(3-Aminomethyl-2-methyl-phenyl)-acenaphthylen-1-yl]-2-methyl-benzylamine
• 英文别名: [3-[2-[3-(Aminomethyl)-2-methylphenyl]acenaphthylen-1-yl]-2-methylphenyl]methanamine；[3-[2-[3-(aminomethyl)-2-methylphenyl]acenaphthylen-1-yl]-2-methylphenyl]methanamine
• CAS: 127158-74-1
• 化学式: C₂₈H₂₆N₂
• 分子量: 390.528
• InChiKey: PHORNDOCEOHLFO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  52
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-[2-(3-Aminomethyl-2-methyl-phenyl)-acenaphthylen-1-yl]-2-methyl-benzylamine 生成 1,2-bis<3-(bromomethyl)-2-methylphenyl>acenaphthylene
  参考文献：
  名称：

  Synthesis and Diatropicity of trans-10b,10c-Dimethylacenaphthyleno[1,2:e]-10b,10c-dihydropyrene:  A Model Aromatic Molecule To Verify the Effect of Conjugation on the Diatropicity of an Annulene

  摘要：

  The title compound 11 was synthesized from acenaphthenequinone in 11 steps with an overall yield of ca. 1.3%. Photochemical desulfurization of the thiacyclophanene 24 afforded the cyclophanene 28. Photochemical isomerization of 28 to the tetrahydropyrene derivative 32 followed by DDQ oxidation gave the desired dihydropyrene 11. Compound 11 is found to sustain only about 85% of the ring current of the parent dihydropyrene 1. On the basis of our results, a significant effect on the diatropicity of the 14 pi annulene in 11 due to its conjugation with a naphthalene moiety is verified. A correlation between theoretically calculated bond orders and experimentally observed coupling constants for selected bonds in 11 indicates that the inductive effect, relative to the resonance effect, plays a major role in the net effect of conjugation observed in 11. Among several derivatives of dihydropyrene 1, a linear relationship is observed for an empirical correlation between the methyl chemical shifts and the corresponding Dewar resonance energies associated with the benzenoid systems in conjugation with 1. This may serve as a method to estimate the resonance energies of other aromatic systems relative to that of benzene. Compound 11 underwent. electrophilic nitration, acetylation, and bromination readily under mild conditions. The electrophiles reacted selectively with the dihydropyrene system in 11 and not the acenaphthylene moiety in conjugation.

  DOI：

  10.1021/jo961237+
• 作为产物：
  描述：

  2,6-二氯甲苯 在 lithium aluminium tetrahydride 、 硫酸 、 碘 、 magnesium 、 溶剂黄146 、 1,2-二溴乙烷 作用下， 以 四氢呋喃 、 溶剂黄146 为溶剂， 反应 27.75h， 生成 3-[2-(3-Aminomethyl-2-methyl-phenyl)-acenaphthylen-1-yl]-2-methyl-benzylamine
  参考文献：
  名称：

  Synthesis and Diatropicity of trans-10b,10c-Dimethylacenaphthyleno[1,2:e]-10b,10c-dihydropyrene:  A Model Aromatic Molecule To Verify the Effect of Conjugation on the Diatropicity of an Annulene

  摘要：

  The title compound 11 was synthesized from acenaphthenequinone in 11 steps with an overall yield of ca. 1.3%. Photochemical desulfurization of the thiacyclophanene 24 afforded the cyclophanene 28. Photochemical isomerization of 28 to the tetrahydropyrene derivative 32 followed by DDQ oxidation gave the desired dihydropyrene 11. Compound 11 is found to sustain only about 85% of the ring current of the parent dihydropyrene 1. On the basis of our results, a significant effect on the diatropicity of the 14 pi annulene in 11 due to its conjugation with a naphthalene moiety is verified. A correlation between theoretically calculated bond orders and experimentally observed coupling constants for selected bonds in 11 indicates that the inductive effect, relative to the resonance effect, plays a major role in the net effect of conjugation observed in 11. Among several derivatives of dihydropyrene 1, a linear relationship is observed for an empirical correlation between the methyl chemical shifts and the corresponding Dewar resonance energies associated with the benzenoid systems in conjugation with 1. This may serve as a method to estimate the resonance energies of other aromatic systems relative to that of benzene. Compound 11 underwent. electrophilic nitration, acetylation, and bromination readily under mild conditions. The electrophiles reacted selectively with the dihydropyrene system in 11 and not the acenaphthylene moiety in conjugation.

  DOI：

  10.1021/jo961237+

文献信息

• Synthesis and Diatropicity of <i>trans</i>-10b,10c-Dimethylacenaphthyleno[1,2:<i>e</i>]-10b,10c-dihydropyrene:  A Model Aromatic Molecule To Verify the Effect of Conjugation on the Diatropicity of an Annulene
  作者：Yee-Hing Lai、Pu Chen、Thomas W. Dingle

  DOI：10.1021/jo961237+

  日期：1997.2.1

  The title compound 11 was synthesized from acenaphthenequinone in 11 steps with an overall yield of ca. 1.3%. Photochemical desulfurization of the thiacyclophanene 24 afforded the cyclophanene 28. Photochemical isomerization of 28 to the tetrahydropyrene derivative 32 followed by DDQ oxidation gave the desired dihydropyrene 11. Compound 11 is found to sustain only about 85% of the ring current of the parent dihydropyrene 1. On the basis of our results, a significant effect on the diatropicity of the 14 pi annulene in 11 due to its conjugation with a naphthalene moiety is verified. A correlation between theoretically calculated bond orders and experimentally observed coupling constants for selected bonds in 11 indicates that the inductive effect, relative to the resonance effect, plays a major role in the net effect of conjugation observed in 11. Among several derivatives of dihydropyrene 1, a linear relationship is observed for an empirical correlation between the methyl chemical shifts and the corresponding Dewar resonance energies associated with the benzenoid systems in conjugation with 1. This may serve as a method to estimate the resonance energies of other aromatic systems relative to that of benzene. Compound 11 underwent. electrophilic nitration, acetylation, and bromination readily under mild conditions. The electrophiles reacted selectively with the dihydropyrene system in 11 and not the acenaphthylene moiety in conjugation.