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tert-butyl (Z)-2-[amino(phenyl)methylene]-3-oxobutanoate | 1629803-11-7

中文名称
——
中文别名
——
英文名称
tert-butyl (Z)-2-[amino(phenyl)methylene]-3-oxobutanoate
英文别名
——
tert-butyl (Z)-2-[amino(phenyl)methylene]-3-oxobutanoate化学式
CAS
1629803-11-7
化学式
C15H19NO3
mdl
——
分子量
261.321
InChiKey
YEHTXVATAOHCOH-SEYXRHQNSA-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

反应信息

  • 作为反应物:
    描述:
    tert-butyl (Z)-2-[amino(phenyl)methylene]-3-oxobutanoate(二氯碘)-苯 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.42h, 以79%的产率得到tert-butyl (E)-2-chloro-2-[(chloroimino)(phenyl)methyl]-3-oxobutanoate
    参考文献:
    名称:
    PhICl2-Mediated Conversion of Enamines into α,N-Dichloroimines and Their Reverse Conversion Mediated by Zinc in Methanol
    摘要:
    Treatment of enamine compounds with iodobenzene dichloride (PhICl2) conveniently gives a variety of alpha,N-dichloroimines in high yields. This approach allows the double insertion of the chloro moiety, which is postulated to take place via the iodobenzene dichloride mediated oxidative alpha-chlorination of the enamine substrates followed by further N-chlorination of the imine intermediates. Furthermore, the obtained alpha,N-dichloroimines could be converted reversely into the original enamines under reductive conditions using zinc in methanol.
    DOI:
    10.1055/s-0033-1341067
  • 作为产物:
    描述:
    tert-butyl (E)-2-chloro-2-[(chloroimino)(phenyl)methyl]-3-oxobutanoate 作用下, 以 甲醇 为溶剂, 以73%的产率得到tert-butyl (Z)-2-[amino(phenyl)methylene]-3-oxobutanoate
    参考文献:
    名称:
    PhICl2-Mediated Conversion of Enamines into α,N-Dichloroimines and Their Reverse Conversion Mediated by Zinc in Methanol
    摘要:
    Treatment of enamine compounds with iodobenzene dichloride (PhICl2) conveniently gives a variety of alpha,N-dichloroimines in high yields. This approach allows the double insertion of the chloro moiety, which is postulated to take place via the iodobenzene dichloride mediated oxidative alpha-chlorination of the enamine substrates followed by further N-chlorination of the imine intermediates. Furthermore, the obtained alpha,N-dichloroimines could be converted reversely into the original enamines under reductive conditions using zinc in methanol.
    DOI:
    10.1055/s-0033-1341067
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