4-Methoxy-1-(phenyl-butylamino-methyl)-benzol | 93948-35-7

• 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: 4-Methoxy-1-(phenyl-butylamino-methyl)-benzol
• 英文别名: N-[(4-methoxyphenyl)-phenylmethyl]butan-1-amine
• CAS: 93948-35-7
• 化学式: C₁₈H₂₃NO
• 分子量: 269.387
• InChiKey: XNTLGBFZMMDAEK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  20
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  21.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  N-(p-methoxybenzylidene)butylamine 、 phenylmagnesium bromide 在 1-(三甲基硅基)苯并三氮唑 作用下， 以 乙醚 、 甲苯 为溶剂， 反应 20.0h， 生成 4-Methoxy-1-(phenyl-butylamino-methyl)-benzol
  参考文献：
  名称：

  Preparations of Secondary Amines and .beta.-Amino Esters via Additions of Grignard and Reformatsky Reagents to Imines and by One-Pot Reactions of Primary Amines, Aldehydes, and Grignards

  摘要：

  Additions oi. Grignard and Reformatsky reagents to imines in the presence of 1-(trimethylsilyl)benzotriazole afforded in good yields the corresponding secondary amines and p-amino esters. The procedure is general as imines containing hydrogens a to both carbon and nitrogen can be employed. Extensions of this method to include imines containing other Lewis basic centers, e.g., those derived from furan-, thiophene-, indole-, and p-methoxybenzenecarboxaldehyde, have been successful in avoiding the potential complications which could result from the use of a Lewis acid as the activating : species. The imines need not be isolated, and a one-pot method for the synthesis of secondary amines from aldehydes, primary amines, and Grignard reagents is described.

  DOI：

  10.1021/jo00116a027

文献信息

• Additionen von Organometallverbindungen an die C?N-Bindung
  作者：A. Marxer、M. Horvath

  DOI：10.1002/hlca.19640470421

  日期：——

  The addition of organometallic compounds to SCHIFF bases, hydrazones, and oximes was studied. It is shown that, contrary to statements in the literature, hydra-zones and oximes may give rise to the same type of C-alkylation and C-arylation as already known for SCHIFF bases.

  研究了向SCHIFF碱，和肟中添加有机金属化合物的方法。结果表明，与文献中的陈述相反，水合区和肟可引起与SCHIFF碱已知的相同类型的C-烷基化和C-芳基化。