(4-Benzotriazol-1-ylmethyl-phenyl)-diethyl-amine | 129075-92-9

• 物质功能分类: 有机原料 - 氨基化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并三唑类
• 英文名称: (4-Benzotriazol-1-ylmethyl-phenyl)-diethyl-amine
• 英文别名: 4-(1H-1,2,3-Benzotriazol-1-ylmethyl)-N,N-diethylaniline；4-(benzotriazol-1-ylmethyl)-N,N-diethylaniline
• CAS: 129075-92-9
• 化学式: C₁₇H₂₀N₄
• 分子量: 280.373
• InChiKey: JEVJEAIDFYWTOE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  34
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (4-Benzotriazol-1-ylmethyl-phenyl)-diethyl-amine 在 盐酸 、 正丁基锂 作用下， 以 甲醇 、 水 为溶剂， 反应 19.0h， 生成 1-((4-(N,N-Dimethylamino)phenyl)(indol-3-yl)methyl)cyclohexan-1-ol
  参考文献：
  名称：

  Benzotriazole as a synthetic auxiliary: advantageous syntheses of substituted diarylmethanes and heterocyclic analogs

  摘要：

  4-(Benzotriazol-1-ylmethyl)-N,N-dimethylaniline (1b) can be substituted at the CH2 link via lithiation. Both the parent and substituted derivatives react with a variety of electron-rich benzenoid and heteroaromatic compounds in a novel approach to leuco dyes. Other 4-(benzotriazol-1-ylmethyl)anilines react similarly.

  DOI：

  10.1021/jo00014a014
• 作为产物：
  描述：

  1H-苯并三唑-1-甲醇 、 N,N-二乙基苯胺 以 溶剂黄146 为溶剂， 反应 0.07h， 以52%的产率得到N1,n1-二乙基-4-[4-(二乙基氨基)苄基]苯胺
  参考文献：
  名称：

  Benzotriazole Mediated Synthesis of Methylenebisanilines

  摘要：

  亚甲基双苯胺和亚甲基双(N,N-二烷基苯胺)是由 1-羟甲基苯并三唑与苯胺和 N,N-二烷基苯胺在酸性条件下反应制备的。通过分离中间体 4-(苯并三唑-1-基甲基)苯胺和 N,N-二烷基类似物以及它们与苯胺的反应，可以有效地制备这两类产品的对称和不对称成员。

  DOI：

  10.1055/s-1990-26873

文献信息

• Benzotriazole: A novel synthetic auxiliary
  作者：Alan R. Katritzky、Stanislaw Rachwal、Gregory J. Hitchings

  DOI：10.1016/s0040-4020(01)87080-0

  日期：1991.1

  eliminated to form products of type Bt-CHR-NR′R″. The latter are versatile intermediates for the preparation of primary, secondary, and tertiary amines and in the alkylation of hydroxylamines, hydrazines, amides, thioamides, and sulfonamides. Polyfunctional amines and other polyfunctional compounds can also be prepared, and they enable significant extending of Mannich reaction.

  苯并三唑和醛可逆地反应生成加成产物：在胺和其他NH化合物存在下，可以消除水形成Bt-CHR-NR'R''型产物。后者是用于制备伯胺，仲胺和叔胺以及羟胺，肼，酰胺，硫酰胺和磺酰胺烷基化的通用中间体。也可以制备多官能胺和其他多官能化合物，它们使曼尼希反应显着扩展。
• Novel routes to 4-substituted N,N-dialkylanilines, N-alkylanilines and anilines
  作者：Alan R. Katritzky、Hengyuan Lang、Xiangfu Lan

  DOI：10.1016/s0040-4020(01)87221-5

  日期：1993.8

  N-dialkylanilines, -N-alkylanilines, -anilines and some substituted analogs obtained via lithiation are converted by lithium aluminum hydride or Grignard reagents into 4-substituted N,N-dialkylanilines, N-alkylanilines and anilines, respectively, in good yields.

  通过氢化锂铝或格氏试剂将4-（苯并三唑-1-基甲基）-N，N-二烷基苯胺，-N-烷基苯胺，-苯胺和一些通过锂化获得的取代类似物通过氢化锂铝或格氏试剂转化为4-取代的N，N-二烷基苯胺，N -烷基苯胺和苯胺分别具有良好的收率。
• Trans-Selective Olefination of Carbonyl Compounds by Low-Valent Titanium-Mediated Dehydroxybenzotriazolylation
  作者：Alan R. Katritzky、Dai Cheng、Scott A. Henderson、Jianqing Li

  DOI：10.1021/jo980616v

  日期：1998.9.1

  Lithiation with n-butyllithium of a variety of benzotriazole derivatives 1a-f and 5a-d, all containing a proton alpha to the benzotriazolyl moiety, gave anions which underwent addition to aliphatic, aromatic, and alpha,beta-unsaturated aldehydes and cyclic and acyclic ketones. The resultant N-(beta-hydroxyalkyl)benzotriazole derivatives 3a-m, 6a-g, 9a-d, and 10a were dehydroxybenzotriazolylated when treated with low-valent titanium to give alkenes 4a-m, dienes 7a-j, and triene 11a, with selectivity for the trans isomers without separation of diastereoisomeric intermediates. This method offers an alternative to the three most frequently used methods for the formation of alkenes from carbonyl compounds-the Wittig, Peterson, and Julia reactions-especially in the formation of tri- and tetrasubstituted alkenes.
• KATRIZKY, ALAN R.;LAN, XIANGFU;LAM, JAMSHED N., J. ORG. CHEM., 56,(1991) N4, C. 4397-4403
  作者：KATRIZKY, ALAN R.、LAN, XIANGFU、LAM, JAMSHED N.

  DOI：——

  日期：——
• Benzotriazole as a synthetic auxiliary: advantageous syntheses of substituted diarylmethanes and heterocyclic analogs
  作者：Alan R. Katritzky、Xiangfu Lan、Jamshed N. Lam

  DOI：10.1021/jo00014a014

  日期：1991.7

  4-(Benzotriazol-1-ylmethyl)-N,N-dimethylaniline (1b) can be substituted at the CH2 link via lithiation. Both the parent and substituted derivatives react with a variety of electron-rich benzenoid and heteroaromatic compounds in a novel approach to leuco dyes. Other 4-(benzotriazol-1-ylmethyl)anilines react similarly.