2-nitro-N-(3-phenylmethoxyphenyl)benzenesulfonamide | 1022805-64-6

• 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: 2-nitro-N-(3-phenylmethoxyphenyl)benzenesulfonamide
• CAS: 1022805-64-6
• 化学式: C₁₉H₁₆N₂O₅S
• 分子量: 384.412
• InChiKey: ZNPYAGUQQIABHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  27
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  110
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-nitro-N-(3-phenylmethoxyphenyl)benzenesulfonamide 在 五甲基苯 、 三氯化硼 作用下， 以 二氯甲烷 为溶剂， 反应 0.33h， 以93%的产率得到N-(3-hydroxyphenyl)-2-nitrobenzenesulfonamide
  参考文献：
  名称：

  Mild Debenzylation of Aryl Benzyl Ether with BCl₃ in the Presence of Pentamethylbenzene as a Non-Lewis-Basic Cation Scavenger

  摘要：

  Scope and limitations of the debenzylation conditions for aryl benzyl ether, which was developed during our synthetic studies on yatakemycin, were investigated. The chemoselective debenzylation proceeds at low temperature with a combination of BCl(3) and pentamethylbenzene as a cation scavenger in the presence of various functional groups.

  DOI：

  10.1055/s-2008-1077980

文献信息

• Mild Debenzylation of Aryl Benzyl Ether with BCl₃ in the Presence of Pentamethylbenzene as a Non-Lewis-Basic Cation Scavenger
  作者：Hidetoshi Tokuyama、Kentaro Okano、Kei-ichiro Okuyama、Tohru Fukuyama

  DOI：10.1055/s-2008-1077980

  日期：——

  Scope and limitations of the debenzylation conditions for aryl benzyl ether, which was developed during our synthetic studies on yatakemycin, were investigated. The chemoselective debenzylation proceeds at low temperature with a combination of BCl(3) and pentamethylbenzene as a cation scavenger in the presence of various functional groups.