3-ethyl-4-phenyl-1-tosyl-1H-pyrrole | 1584705-45-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 3-ethyl-4-phenyl-1-tosyl-1H-pyrrole
• 英文别名: 3-Ethyl-1-(4-methylphenyl)sulfonyl-4-phenylpyrrole；3-ethyl-1-(4-methylphenyl)sulfonyl-4-phenylpyrrole
• CAS: 1584705-45-2
• 化学式: C₁₉H₁₉NO₂S
• 分子量: 325.431
• InChiKey: IFSPCJTZTCQIHY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  47.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole 、 1-ethoxybut-1-ene 在 dirhodium tetraacetate 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 5.0h， 以86%的产率得到3-ethyl-4-phenyl-1-tosyl-1H-pyrrole
  参考文献：
  名称：

  Synthesis of Pyrroles from Terminal Alkynes, N-Sulfonyl Azides, and Alkenyl Alkyl Ethers through 1-Sulfonyl-1,2,3-triazoles

  摘要：

  A method for synthesis of substituted pyrroles has been developed. 1-Sulfonyl-1,2,3-triazoles generated from terminal alkynes gave alpha-imino rhodium carbene complexes, which when reacted with alkenyl alkyl ethers afforded substituted pyrroles. The method can be efficiently applied to a one-pot sequential reaction starting from terminal alkynes.

  DOI：

  10.1021/ol500718s

文献信息

• Synthesis of Pyrroles from Terminal Alkynes, <i>N</i>-Sulfonyl Azides, and Alkenyl Alkyl Ethers through 1-Sulfonyl-1,2,3-triazoles
  作者：Cheol-Eui Kim、Sangjune Park、Dahan Eom、Boram Seo、Phil Ho Lee

  DOI：10.1021/ol500718s

  日期：2014.4.4

  A method for synthesis of substituted pyrroles has been developed. 1-Sulfonyl-1,2,3-triazoles generated from terminal alkynes gave alpha-imino rhodium carbene complexes, which when reacted with alkenyl alkyl ethers afforded substituted pyrroles. The method can be efficiently applied to a one-pot sequential reaction starting from terminal alkynes.