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4-(4-benzyloxyphenyl)-1-phenyl-2-butyn-1-one | 1149391-17-2

中文名称
——
中文别名
——
英文名称
4-(4-benzyloxyphenyl)-1-phenyl-2-butyn-1-one
英文别名
1-Phenyl-4-(4-phenylmethoxyphenyl)but-2-yn-1-one
4-(4-benzyloxyphenyl)-1-phenyl-2-butyn-1-one化学式
CAS
1149391-17-2
化学式
C23H18O2
mdl
——
分子量
326.395
InChiKey
IGEKZORUAQRAJD-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):
    5.6
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1-苯基-2-丙炔-1-酮4-苄氧基氯化苄copper(l) iodide四丁基碘化铵potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 24.0h, 以60%的产率得到4-(4-benzyloxyphenyl)-1-phenyl-2-butyn-1-one
    参考文献:
    名称:
    Operationally Simple Copper-Promoted Coupling of Terminal Alkynes with Benzyl Halides
    摘要:
    Benzyl chlorides and bromides are shown to undergo copper-promoted coupling with a variety of terminal alkynes including, for the first time, electron-poor acetylenes such as methyl propiolate. The reaction permits easy access to a wide range of (functionalized) benzyl-substituted propiolates (as well as several related alkynes) from commercially available benzyl halides. These products should in turn function as useful building blocks for the synthesis of previously inaccessible (functionalized) benzyl-substituted heterocycles.
    DOI:
    10.1021/jo900444x
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文献信息

  • Operationally Simple Copper-Promoted Coupling of Terminal Alkynes with Benzyl Halides
    作者:Katherine A. Davies、Ryan C. Abel、Jeremy E. Wulff
    DOI:10.1021/jo900444x
    日期:2009.5.15
    Benzyl chlorides and bromides are shown to undergo copper-promoted coupling with a variety of terminal alkynes including, for the first time, electron-poor acetylenes such as methyl propiolate. The reaction permits easy access to a wide range of (functionalized) benzyl-substituted propiolates (as well as several related alkynes) from commercially available benzyl halides. These products should in turn function as useful building blocks for the synthesis of previously inaccessible (functionalized) benzyl-substituted heterocycles.
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