2-Naphthalen-1-yl-2-pyrrolidin-1-ylacetonitrile | 1157424-00-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-Naphthalen-1-yl-2-pyrrolidin-1-ylacetonitrile
• CAS: 1157424-00-4
• 化学式: C₁₆H₁₆N₂
• mdl: MFCD12064529
• 分子量: 236.316
• InChiKey: LDKFMXNFRCMYJL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.312
• 拓扑面积：
  27
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-萘甲醛 在 2-乙基-己酸稀土盐 、 copper(II) bis(trifluoromethanesulfonate) 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 18.58h， 生成 2-Naphthalen-1-yl-2-pyrrolidin-1-ylacetonitrile 、 1-(naphthalen-1-ylmethyl)pyrrolidine-2-carbonitrile
  参考文献：
  名称：

  Redox-Neutral α-Cyanation of Amines

  摘要：

  alpha-Aminonitriles inaccessible by traditional Strecker chemistry are obtained in redox-neutral fashion by direct amine alpha-cyanation/N-alkylation or alternatively, alpha-aminonitrile isomerization. These unprecedented transformations are catalyzed by simple carboxylic acids.

  DOI：

  10.1021/ja308009g

文献信息

• Efficient Co(ii) heterogeneously catalysed synthesis of α-aminonitriles at room temperature via Strecker-type reactions
  作者：Fatemeh Rajabi、Sara Ghiassian、Mohammad Reza Saidi

  DOI：10.1039/c0gc00047g

  日期：——

  An environmentally friendly and highly active mesoporous Co(II) complex on mesoporous SBA-15 material could be used as an easily recoverable catalyst for the synthesis of α-aminonitriles from a wide range of aldehydes/ketones and primary or secondary amines with good to excellent conversions yields at room temperature under solventless conditions. The catalyst can be recovered by simple filtration and could be reused at least 10 times without loss of catalytic activity.

  一种环境友好且活性高的介孔Co(II)配合物负载于介孔SBA-15材料上，可作为易于回收的催化剂，用于在无溶剂条件下室温下从广泛范围的醛/酮和伯或仲胺合成α-氨基腈，并具有优良至极佳的转化产率。通过简单过滤即可回收该催化剂，并且至少可重复使用10次而不会损失其催化活性。
• Redox-Neutral α-Cyanation of Amines
  作者：Longle Ma、Weijie Chen、Daniel Seidel

  DOI：10.1021/ja308009g

  日期：2012.9.19

  alpha-Aminonitriles inaccessible by traditional Strecker chemistry are obtained in redox-neutral fashion by direct amine alpha-cyanation/N-alkylation or alternatively, alpha-aminonitrile isomerization. These unprecedented transformations are catalyzed by simple carboxylic acids.