(Z)-2-chloro-1-(4-fluorophenyl)non-1-ene | 934372-15-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (Z)-2-chloro-1-(4-fluorophenyl)non-1-ene
• 英文别名: 1-[(Z)-2-chloronon-1-enyl]-4-fluorobenzene
• CAS: 934372-15-3
• 化学式: C₁₅H₂₀ClF
• 分子量: 254.775
• InChiKey: SWUJZDRBEVIFGD-OWBHPGMISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  17
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (Z)-2-chloro-1-(4-fluorophenyl)non-1-ene 、 烯丙苯 在 tris(dibenzylideneacetone)dipalladium (0) 9-borabicyclo[3.3.1]nonane dimer 、 potassium fluoride 、 potassium phosphate 、 2-(二环己基膦基)联苯 作用下， 以 四氢呋喃 为溶剂， 反应 96.0h， 以74%的产率得到(Z)-2-(3-phenylpropyl)-1-(4-fluorophenyl)non-1-ene
  参考文献：
  名称：

  Suzuki−Miyaura Cross-Coupling of 1,1-Dichloro-1-alkenes with 9-Alkyl-9-BBN

  摘要：

  We addressed an unexplored application of the Suzuki-Miyaura protocol to the cross-coupling of 1,1-dichloro-1-alkenes with 9-alkyl-9-BBN. The use of bisphosphine ligands with a large P-Pd-P bite angle allowed us to synthesize Z-chlorinated internal alkenes in good yields resulting from a selective monocoupling process, a recurrent challenge with 1,1-dichloro-1-alkenes. Moreover, these monochlorinated olefins could be further transformed providing stereospecifically trisubstituted olefins.

  DOI：

  10.1021/jo061908w
• 作为产物：
  描述：

  1-(4-fluorophenyl)-2,2,2-trichloroethanol 在 9-borabicyclo[3.3.1]nonane dimer 、 溶剂黄146 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 锌 作用下， 以 四氢呋喃 为溶剂， 反应 41.0h， 生成 (Z)-2-chloro-1-(4-fluorophenyl)non-1-ene
  参考文献：
  名称：

  Suzuki−Miyaura Cross-Coupling of 1,1-Dichloro-1-alkenes with 9-Alkyl-9-BBN

  摘要：

  We addressed an unexplored application of the Suzuki-Miyaura protocol to the cross-coupling of 1,1-dichloro-1-alkenes with 9-alkyl-9-BBN. The use of bisphosphine ligands with a large P-Pd-P bite angle allowed us to synthesize Z-chlorinated internal alkenes in good yields resulting from a selective monocoupling process, a recurrent challenge with 1,1-dichloro-1-alkenes. Moreover, these monochlorinated olefins could be further transformed providing stereospecifically trisubstituted olefins.

  DOI：

  10.1021/jo061908w

文献信息

• Suzuki−Miyaura Cross-Coupling of 1,1-Dichloro-1-alkenes with 9-Alkyl-9-BBN
  作者：Frédéric Liron、Céline Fosse、Alban Pernolet、Emmanuel Roulland

  DOI：10.1021/jo061908w

  日期：2007.3.1

  We addressed an unexplored application of the Suzuki-Miyaura protocol to the cross-coupling of 1,1-dichloro-1-alkenes with 9-alkyl-9-BBN. The use of bisphosphine ligands with a large P-Pd-P bite angle allowed us to synthesize Z-chlorinated internal alkenes in good yields resulting from a selective monocoupling process, a recurrent challenge with 1,1-dichloro-1-alkenes. Moreover, these monochlorinated olefins could be further transformed providing stereospecifically trisubstituted olefins.