(E)-7,7,7-trifluorohept-5-en-1-yl dimethylcarbamate | 1415585-57-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (E)-7,7,7-trifluorohept-5-en-1-yl dimethylcarbamate
• 英文别名: [(E)-7,7,7-trifluorohept-5-enyl] N,N-dimethylcarbamate
• CAS: 1415585-57-7
• 化学式: C₁₀H₁₆F₃NO₂
• 分子量: 239.238
• InChiKey: MZJHYDBNAOJPGD-FNORWQNLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  16
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  29.5
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  三氟碘甲烷 、 hex-5-enyl N,N-dimethylcarbamate 在 tris(1,10-phenanthroline)ruthenium(II) dichloride 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 乙腈 为溶剂， 以80%的产率得到(E)-7,7,7-trifluorohept-5-en-1-yl dimethylcarbamate
  参考文献：
  名称：

  Trifluoromethylation of Alkenes by Visible Light Photoredox Catalysis

  摘要：

  A method for trifluoromethylation of alkenes has been developed employing visible light photoredox catalysis with CF3I, Ru(Phen)(3)Cl-2, and DBU. This process works especially well for terminal alkenes to give alkenyl-CF3 products with only E-stereochemistry. The mild reaction conditions enable the trifluoromethylation of a range of alkenes that bear various functional groups.

  DOI：

  10.1021/jo3022346

文献信息

• Controlled Trifluoromethylation Reactions of Alkynes through Visible-Light Photoredox Catalysis
  作者：Naeem Iqbal、Jaehun Jung、Sehyun Park、Eun Jin Cho

  DOI：10.1002/anie.201308735

  日期：2014.1.7

  The control of a reaction that can form multiple products is a highly attractive and challenging concept in synthetic chemistry. A set of valuable CF3‐containing molecules, namely trifluoromethylated alkenyl iodides, alkenes, and alkynes, were selectively generated from alkynes and CF3I by environmentally benign and efficient visible‐light photoredox catalysis. Subtle differences in the combination

  在合成化学中，控制可形成多种产物的反应是一个极具吸引力和挑战性的概念。通过对环境无害且有效的可见光光氧化还原催化作用，从炔烃和CF 3 I选择性地生成了一组有价值的含CF 3分子，即三氟甲基化的烯基碘，烯烃和炔烃。催化剂，碱和溶剂的组合之间存在细微差异，因此可以控制炔烃与CF 3 I之间反应的反应性和选择性。
• Trifluoromethylation of Alkenes by Visible Light Photoredox Catalysis
  作者：Naeem Iqbal、Sungkyu Choi、Eunjin Kim、Eun Jin Cho

  DOI：10.1021/jo3022346

  日期：2012.12.21

  A method for trifluoromethylation of alkenes has been developed employing visible light photoredox catalysis with CF3I, Ru(Phen)(3)Cl-2, and DBU. This process works especially well for terminal alkenes to give alkenyl-CF3 products with only E-stereochemistry. The mild reaction conditions enable the trifluoromethylation of a range of alkenes that bear various functional groups.