3-(nonyloxy)propanenitrile | 5327-01-5

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 3-(nonyloxy)propanenitrile
• 英文别名: 3-nonyloxy-propionitrile；3-nonoxypropanenitrile
• CAS: 5327-01-5
• 化学式: C₁₂H₂₃NO
• 分子量: 197.321
• InChiKey: AZDYBNAAPZWEMG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  14
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  33
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2926909090

反应信息

• 作为反应物：
  描述：

  3-(nonyloxy)propanenitrile 在 镍 氢气 作用下， 以 乙醇 为溶剂， 生成 Bis-(3-nonyloxy-propyl)-amin
  参考文献：
  名称：

  Gaiffe,A.; Launay,C., Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1968, vol. 266, p. 471 - 472

  摘要：

  DOI：
• 作为产物：
  描述：

  1-壬醇 以91%的产率得到
  参考文献：
  名称：

  SUN, XIAOYUN;PENG, GUICHUN, XUASYUEH TUNBAO,(1990) N, S. 48-49

  摘要：

  DOI：

文献信息

• KO <i>t</i> Bu‐Catalyzed Michael Addition Reactions Under Mild and Solvent‐Free Conditions
  作者：Subramanian Thiyagarajan、Varadhan Krishnakumar、Chidambaram Gunanathan

  DOI：10.1002/asia.201901647

  日期：2020.2.17

  predominantly catalyze Michael addition reactions. Inorganic and organic base‐catalyzed Michael addition reactions have been reported. However, known base‐catalyzed reactions suffer from the requirement of solvents, additives, high pressure and also side‐reactions. Herein, we demonstrate a mild and environmentally friendly strategy of readily available KOtBu‐catalyzed Michael addition reactions. This simple

  设计的过渡金属络合物主要催化迈克尔加成反应。无机和有机碱催化的迈克尔加成反应已有报道。但是，已知的碱催化反应需要溶剂，添加剂，高压以及副反应。在此，我们展示了一种易于使用的KO t的温和且环保的策略Bu催化Michael加成反应。这种简单的无机碱可有效催化未开发的丙烯腈，酯和酰胺与（氧杂，氮杂和硫杂）杂原子亲核试剂的迈克尔加成反应。该催化过程在无溶剂条件和室温下进行。值得注意的是，该协议提供了一种简便的操作程序，宽泛的底物范围，出色的选择性，反应可扩展性和出色的TON（> 9900）。初步的机理研究表明，该反应遵循离子机理。使用该催化方案证明了丙嗪的正式合成。
• Gaiffe,A.; Launay,C., Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1967, vol. 264, p. 1496 - 1497
  作者：Gaiffe,A.、Launay,C.

  DOI：——

  日期：——
• Photocatalyzed [2 + 2 + 2]-Cycloaddition of Nitriles with Acetylene:  An Effective Method for the Synthesis of 2-Pyridines under Mild Conditions
  作者：Barbara Heller、Bernd Sundermann、Helmut Buschmann、Hans-Joachim Drexler、Jingsong You、Ulrike Holzgrabe、Eberhard Heller、Günther Oehme

  DOI：10.1021/jo011032n

  日期：2002.6.1

  The photocatalyzed [2 + 2 + 2]-cycloaddition of nitriles with 2 equiv of acetylene to 2-pyridines can be carried out under mild conditions and represents a valuable extension to common synthetical methods. For the ideal wavelength range (350-500 nm), lamps as well as sunlight can be used. Working at room temperature and in organic solvents such as toluene or hexane as well as in water gives satisfying results in many cases. However, it is also possible to vary the solvent and the reaction temperature of the photocatalyzed synthesis and to choose, with respect to the specific substrate, specific requirements for this particular reaction and general requirements of the method. This simple and selective method derives its potential mainly from the large variety of applicable nitriles. Suitable substrates include (functionalized) aliphatic and aromatic nitriles as well as cyanamides derived from secondary amines.
• Gaiffe,A.; Launay,C., Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1968, vol. 266, p. 1379 - 1380
  作者：Gaiffe,A.、Launay,C.

  DOI：——

  日期：——
• SUN, XIAOYUN;PENG, GUICUN, INYUN XUASYUEH, 7,(1990) N, S. 88-90
  作者：SUN, XIAOYUN、PENG, GUICUN

  DOI：——

  日期：——