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1-(3,3-dimethyl-2-oxobutyl)piperidine-2,6-dione | 1250217-07-2

中文名称
——
中文别名
——
英文名称
1-(3,3-dimethyl-2-oxobutyl)piperidine-2,6-dione
英文别名
——
1-(3,3-dimethyl-2-oxobutyl)piperidine-2,6-dione化学式
CAS
1250217-07-2
化学式
C11H17NO3
mdl
——
分子量
211.261
InChiKey
AIIGCRFVGGRPBM-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    54.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    戊二酰亚胺 、 3,3-dimethyl-1-butynyl[tri(4-methylphenyl)]bismuthonium tetrafluoroborate 在 三乙胺 、 copper(I) bromide 、 盐酸 作用下, 以 二氯甲烷 为溶剂, 反应 5.0h, 以38%的产率得到N-(对甲基苯基)戊二酰亚胺
    参考文献:
    名称:
    N-Alkynyl Imides (Ynimides): Synthesis and Use as a Variant of Highly Labile Ethynamine
    摘要:
    This study describes the first reliable synthesis of N-alkynyl imides (ynimides). This was accomplished with a copper-catalyzed coupling reaction between alkynyl(triaryl)bismuthonium salts and five-membered imides. We also found that it was possible to utilize N-ethynyl phthalimide as a variant of the highly labile ethynamine. 4-Amino-1,2,3-triazole was successfully obtained via the CuAAC reaction of N-ethynyl phthalimide with azide followed by hydrazinolysis of the phthaloyl protecting group.
    DOI:
    10.1021/ol2014973
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文献信息

  • <i>N</i>-Alkynyl Imides (Ynimides): Synthesis and Use as a Variant of Highly Labile Ethynamine
    作者:Takuya Sueda、Ayumi Oshima、Naoki Teno
    DOI:10.1021/ol2014973
    日期:2011.8.5
    This study describes the first reliable synthesis of N-alkynyl imides (ynimides). This was accomplished with a copper-catalyzed coupling reaction between alkynyl(triaryl)bismuthonium salts and five-membered imides. We also found that it was possible to utilize N-ethynyl phthalimide as a variant of the highly labile ethynamine. 4-Amino-1,2,3-triazole was successfully obtained via the CuAAC reaction of N-ethynyl phthalimide with azide followed by hydrazinolysis of the phthaloyl protecting group.
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