N-[2-(4-chlorophenoxy)-3-(3-chlorophenyl)-3,4-dihydro-2H-1,3,2-λ5-benzoxazaphosphinin-2-yliden]-N-allyl amine | 1260217-90-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: N-[2-(4-chlorophenoxy)-3-(3-chlorophenyl)-3,4-dihydro-2H-1,3,2-λ5-benzoxazaphosphinin-2-yliden]-N-allyl amine
• CAS: 1260217-90-0
• 化学式: C₂₂H₁₉Cl₂N₂O₂P
• 分子量: 445.285
• InChiKey: DQBJWSDYFMHYSE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.6
• 重原子数：
  29.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  34.06
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为产物：
  描述：

  p-chlorophenyl dichlorophosphite 在 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 生成 N-[2-(4-chlorophenoxy)-3-(3-chlorophenyl)-3,4-dihydro-2H-1,3,2-λ5-benzoxazaphosphinin-2-yliden]-N-allyl amine
  参考文献：
  名称：

  N-[2-(4-卤代苯氧基)-3-(3-氯苯基)-3, 4-dihydro-2H-1,3,2-λ5-benzoxazaphosphinin-2-yliden]-N-取代的合成及光谱表征施陶丁格反应生成的胺

  摘要：

  AbstractThe synthesis of the title compounds was accomplished in four steps. The synthetic route involves the preparation of Schiff's base by reacting salicylaldehyde with m‐chloroaniline in EtOH. The Schiff's base was then reduced with NaBH4/MeOH. In the second step, PCl3 was reacted with p‐chlorophenol/p‐bromophenol in THF in the presence of Et3N to obtain P(III) dichloride derivatives. The reduced Schiff's base and dichloride derivatives were reacted in equimolar quantities in the presence of Et3N in THF to get the cyclized product. Alkyl azides were prepared by reacting alkyl bromides with sodium azide, and then alkyl azides were treated with the cyclized product to obtain the title compounds. The structure of these novel compounds was elucidated by elemental analysis, IR, 1H, 13C, 31P NMR, and mass spectroscopy. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:499–504, 2010; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20639

  DOI：

  10.1002/hc.20639