4-[(2E)-hept-2-en-1-yl]morpholine | 1608131-93-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 恶嗪烷类
• 英文名称: 4-[(2E)-hept-2-en-1-yl]morpholine
• 英文别名: (E)-4-(hept-2-en-1-yl)morpholine；4-[(2e)-Hept-2-en-1-yl]morpholine；4-[(E)-hept-2-enyl]morpholine
• CAS: 1608131-93-6
• 化学式: C₁₁H₂₁NO
• 分子量: 183.294
• InChiKey: NXJFRWLHNMULHT-AATRIKPKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  正丁基氯化镁 、 1-[(2E)-3-chloroprop-2-en-1-yl]morpholine 在 iron(III)-acetylacetonate 作用下， 以 四氢呋喃 、 N-甲基吡咯烷酮 为溶剂， 反应 1.5h， 以84%的产率得到4-[(2E)-hept-2-en-1-yl]morpholine
  参考文献：
  名称：

  Stereoselective synthesis of allylamines by iron-catalyzed cross-coupling of 3-chloroprop-2-en-1-amines with grignard reagents. Synthesis of naftifine

  摘要：

  A general procedure for the synthesis of trans- and cis-allylamines has been developed on the basis of iron-catalyzed cross-coupling of Grignard reagents with stereochemically pure 3-chloroprop-2-en-1-amines prepared by allylation of amines with commercially available 1,3-dichloropropene isomers.

  DOI：

  10.1134/s1070428014030038

文献信息

• Cationic [(Iminophosphine)Nickel(Allyl)]⁺Complexes as the First Example of Nickel Catalysts for Direct Hydroamination of Allenes
  作者：Hosein Tafazolian、Joseph A. R. Schmidt

  DOI：10.1002/chem.201605611

  日期：2017.1.31

  The first example of nickel‐catalyzed hydroamination of allenes is reported. The new cationic [(3‐iminophosphine)nickel(allyl)]+ catalysts have been fully characterized and act regioselectively in the catalytic hydroamination of allenes with secondary amines at room temperature.

  报道了镍催化的丙二烯加氢胺化的第一个例子。新型阳离子[（3-亚氨基膦）镍（烯丙基）] +催化剂已得到充分表征，并在室温下在丙二烯与仲胺的催化加氢胺化反应中具有区域选择性作用。
• Stereoselective synthesis of allylamines by iron-catalyzed cross-coupling of 3-chloroprop-2-en-1-amines with grignard reagents. Synthesis of naftifine
  作者：R. N. Shakhmaev、A. Sh. Sunagatullina、V. V. Zorin

  DOI：10.1134/s1070428014030038

  日期：2014.3

  A general procedure for the synthesis of trans- and cis-allylamines has been developed on the basis of iron-catalyzed cross-coupling of Grignard reagents with stereochemically pure 3-chloroprop-2-en-1-amines prepared by allylation of amines with commercially available 1,3-dichloropropene isomers.