(E)-N-methoxy-N-methyl-3,5-diphenylpent-2-enamide | 1429057-76-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: (E)-N-methoxy-N-methyl-3,5-diphenylpent-2-enamide
• CAS: 1429057-76-0
• 化学式: C₁₉H₂₁NO₂
• 分子量: 295.381
• InChiKey: DOZUFEXYEOWNII-OBGWFSINSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  22
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  29.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (E)-N-methoxy-N-methyl-3,5-diphenylpent-2-enamide 、 苯基溴化镁 以 四氢呋喃 、 乙醚 为溶剂， 反应 1.0h， 以80%的产率得到(E)-1,3,5-triphenyl-2-penten-1-one
  参考文献：
  名称：

  Vinyl Weinreb amides: a versatile alternative to vinyl ketone substrates for the Heck arylation

  摘要：

  This paper describes the use of unsaturated Weinreb amides as excellent substrates for the Heck reaction. Subsequent derivatization of the products with organometallic reagents allowed access to a variety of substituted vinyl ketones that could not have been prepared directly via Heck reaction on unsaturated ketone precursors. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.03.009
• 作为产物：
  描述：

  (E)-5-Phenyl-pent-2-enoic acid methoxy-methyl-amide 、 苯硼酸 在 potassium fluoride 、 阻聚剂701 、 palladium diacetate 、 丙酸 作用下， 反应 4.0h， 以86%的产率得到(E)-N-methoxy-N-methyl-3,5-diphenylpent-2-enamide
  参考文献：
  名称：

  Vinyl Weinreb amides: a versatile alternative to vinyl ketone substrates for the Heck arylation

  摘要：

  This paper describes the use of unsaturated Weinreb amides as excellent substrates for the Heck reaction. Subsequent derivatization of the products with organometallic reagents allowed access to a variety of substituted vinyl ketones that could not have been prepared directly via Heck reaction on unsaturated ketone precursors. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.03.009

文献信息

• Vinyl Weinreb amides: a versatile alternative to vinyl ketone substrates for the Heck arylation
  作者：David B. Baker、Peter T. Gallagher、Timothy J. Donohoe

  DOI：10.1016/j.tet.2013.03.009

  日期：2013.5

  This paper describes the use of unsaturated Weinreb amides as excellent substrates for the Heck reaction. Subsequent derivatization of the products with organometallic reagents allowed access to a variety of substituted vinyl ketones that could not have been prepared directly via Heck reaction on unsaturated ketone precursors. (C) 2013 Elsevier Ltd. All rights reserved.