1-Indol-1-yl-4-(4-methoxyphenoxy)butan-1-ol | 201486-60-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 1-Indol-1-yl-4-(4-methoxyphenoxy)butan-1-ol
• 英文别名: 1-indol-1-yl-4-(4-methoxyphenoxy)butan-1-ol
• CAS: 201486-60-4
• 化学式: C₁₉H₂₁NO₃
• 分子量: 311.381
• InChiKey: GAEPAHWHQULOTI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  23
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  43.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-Indol-1-yl-4-(4-methoxyphenoxy)butan-1-ol 在 氰化钠 作用下， 以 甲醇 为溶剂， 反应 1.0h， 以79%的产率得到4-(4-methoxyphenoxyl)butyraldehyde
  参考文献：
  名称：

  2-(2-Aminophenyl)-acetaldehyde Dimethyl Acetal: A Novel Reagent for the Protection of Carboxylic Acids.

  摘要：

  The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes. (C) 1997 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(97)10491-9
• 作为产物：
  描述：

  2-(2,2-二甲氧基乙基)苯甲酰胺 在 喹啉 、 4-二甲氨基吡啶 、 camphor-10-sulfonic acid 、 二异丁基氢化铝 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 、 甲苯 、 苯 为溶剂， 反应 3.17h， 生成 1-Indol-1-yl-4-(4-methoxyphenoxy)butan-1-ol
  参考文献：
  名称：

  2-(2-Aminophenyl)-acetaldehyde Dimethyl Acetal: A Novel Reagent for the Protection of Carboxylic Acids.

  摘要：

  The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes. (C) 1997 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(97)10491-9

文献信息

• 2-(2-Aminophenyl)-acetaldehyde Dimethyl Acetal: A Novel Reagent for the Protection of Carboxylic Acids.
  作者：Eri Arai、Hidetoshi Tokuyama、Martin S Linsell、Tohru Fukuyama

  DOI：10.1016/s0040-4039(97)10491-9

  日期：1998.1

  The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes. (C) 1997 Elsevier Science Ltd. All rights reserved.