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(2-(N-imidazolinyl)-2-(phenylseleno)ethyl)methylpropanedinitrile | 141439-34-1

中文名称
——
中文别名
——
英文名称
(2-(N-imidazolinyl)-2-(phenylseleno)ethyl)methylpropanedinitrile
英文别名
2-(2-imidazol-1-yl-2-phenylselanylethyl)-2-methylpropanedinitrile
(2-(N-imidazolinyl)-2-(phenylseleno)ethyl)methylpropanedinitrile化学式
CAS
141439-34-1
化学式
C15H14N4Se
mdl
——
分子量
329.263
InChiKey
RYGDQIYDFGJXEU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    536.2±50.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.85
  • 重原子数:
    20.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    65.4
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    1-乙烯基咪唑methyl phenylselenomalonitrile偶氮二异丁腈 作用下, 以 氯仿 为溶剂, 反应 120.0h, 以91%的产率得到(2-(N-imidazolinyl)-2-(phenylseleno)ethyl)methylpropanedinitrile
    参考文献:
    名称:
    Group Transfer Addition Reactions of Methyl (phenylseleno)malononitrile to Alkenes
    摘要:
    Results of a detailed study of group transfer additions of methyl(phenylseleno)propanedinitrile (4) to a wide variety of alkenes are reported. For example, heating of 4 (60 degrees C) with 1-hexene and AIBN produces (2-(phenylseleno)-hexyl)methylpropanedinitrile in 97% yield. Reagent 4 adds in high yields to monosubstituted styrenes, enol ethers, enol acetates, enol sulfides, enamides, and enol imidazoles and carbazoles. Additions to many classes of 1,2-disubstituted alkenes also occur, and modest to good levels of 1,2-asymmetric induction are observed in the selenium transfer step. Oxygen- and sulfur-substituted alkenes produce anti products, and N-substituted alkenes produce syn products. The proposed mechanism involves radical addition followed by phenylselenium group transfer, and it is shown that radical additions to certain classes of disubstituted alkenes can be reversible. Additions to trisubstituted alkenes fair, probably because of this reversibility. Competition studies provide a relative reactivity scale of alkenes toward the electrophilic methylpropanedinitrile radical. Finally, a series of transformations serve to illustrate some synthetic possibilities for the products of these selenium transfer addition reactions.
    DOI:
    10.1021/ja00089a017
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文献信息

  • Additions of malononitrile radicals to alkenes: new examples of 1,2-asymmetric induction in iodine and phenylselenium transfer reactions
    作者:Dennis P. Curran、Gebhard Thoma
    DOI:10.1021/ja00037a080
    日期:1992.5
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