N-[2-(cyclopent-2-enyl)ethyl]-4-chloroaniline | 861104-07-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N-[2-(cyclopent-2-enyl)ethyl]-4-chloroaniline
• 英文别名: 4-chloro-N-(2-cyclopent-2-en-1-ylethyl)aniline
• CAS: 861104-07-6
• 化学式: C₁₃H₁₆ClN
• 分子量: 221.73
• InChiKey: WWEVPYAESYORKU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  15
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N-[2-(cyclopent-2-enyl)ethyl]-4-chloroaniline 、 4-溴苯甲酸叔丁酯 在 tris(dibenzylideneacetone)dipalladium (0) 、 di-tert-butyl(methyl)phosphonium tetrafluoroborate salt 、 sodium t-butanolate 作用下， 以 甲苯 为溶剂， 以71%的产率得到(+/-)-(3aRS,6RS,6aRS)-4-[1-(4-chlorophenyl)octahydrocyclopenta[b]pyrrol-5-yl]benzoic acid tert-butyl ester
  参考文献：
  名称：

  Selective Synthesis of 5- or 6-Aryl Octahydrocyclopenta[b]pyrroles from a Common Precursor through Control of Competing Pathways in a Pd-Catalyzed Reaction

  摘要：

  The Pd/phosphine-catalyzed reaction of 1 with aryl bromides leads to the selective synthesis of either 6-aryl octahydrocyclopenta[b]pyrroles (3), the corresponding 5-aryl isomers 5, diarylamine 2, or hexahydrocyclopenta[b]pyrrole 4 depending on the structure of the phosphine ligand. These transformations are effective with a variety of different aryl bromides and provide 3-5 with excellent levels of diastereo-selectivity (dr >= 20:1). The changes in product distribution are believed to derive from the influence of Pd-catalyst structure on the relative rates of reductive elimination, beta-hydride elimination, alkene insertion, and alkene displacement processes in a mechanistically complex reaction. The effect of phosphine ligand structure on product distribution is described in detail, along with analysis of a proposed mechanism for these transformations.

  DOI：

  10.1021/ja0430346
• 作为产物：
  描述：

  2-环戊烯基-1-乙酸 在 lithium aluminium tetrahydride 、 N,N'-羰基二咪唑 作用下， 以 四氢呋喃 、 乙醚 为溶剂， 反应 26.0h， 生成 N-[2-(cyclopent-2-enyl)ethyl]-4-chloroaniline
  参考文献：
  名称：

  Selective Synthesis of 5- or 6-Aryl Octahydrocyclopenta[b]pyrroles from a Common Precursor through Control of Competing Pathways in a Pd-Catalyzed Reaction

  摘要：

  The Pd/phosphine-catalyzed reaction of 1 with aryl bromides leads to the selective synthesis of either 6-aryl octahydrocyclopenta[b]pyrroles (3), the corresponding 5-aryl isomers 5, diarylamine 2, or hexahydrocyclopenta[b]pyrrole 4 depending on the structure of the phosphine ligand. These transformations are effective with a variety of different aryl bromides and provide 3-5 with excellent levels of diastereo-selectivity (dr >= 20:1). The changes in product distribution are believed to derive from the influence of Pd-catalyst structure on the relative rates of reductive elimination, beta-hydride elimination, alkene insertion, and alkene displacement processes in a mechanistically complex reaction. The effect of phosphine ligand structure on product distribution is described in detail, along with analysis of a proposed mechanism for these transformations.

  DOI：

  10.1021/ja0430346