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(E)-1-(3-(1-phenylprop-1-en-2-yl)furan-2-yl)ethanone | 1228117-80-3

中文名称
——
中文别名
——
英文名称
(E)-1-(3-(1-phenylprop-1-en-2-yl)furan-2-yl)ethanone
英文别名
1-[3-[(E)-1-phenylprop-1-en-2-yl]furan-2-yl]ethanone
(E)-1-(3-(1-phenylprop-1-en-2-yl)furan-2-yl)ethanone化学式
CAS
1228117-80-3
化学式
C15H14O2
mdl
——
分子量
226.275
InChiKey
HSIQRFUBJCPUAC-ZHACJKMWSA-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):
    3.9
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    30.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-苯基-1-丙炔2-乙酰基呋喃 在 tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate 、 三甲基乙酰氯 作用下, 以 醋酸异丙酯 为溶剂, 反应 16.0h, 以91%的产率得到(E)-1-(3-(1-phenylprop-1-en-2-yl)furan-2-yl)ethanone
    参考文献:
    名称:
    Rhodium(III)-Catalyzed Intermolecular Hydroarylation of Alkynes
    摘要:
    The rhodium(III)-catalyzed hydroarylation of internal alkynes is described. Good yields are obtained for a variety of alkynes, and excellent regioselectivity is observed for unsymmetrically substituted alkynes. The reaction also gives good yields for a range of arenes. Preliminary mechanistic investigations suggest that this reaction proceeds through arene metalation with the cationic rhodium catalyst, which enables challenging intermolecular reactivity.
    DOI:
    10.1021/ja103080d
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文献信息

  • Rhodium(III)-Catalyzed Intermolecular Hydroarylation of Alkynes
    作者:Derek J. Schipper、Marieke Hutchinson、Keith Fagnou
    DOI:10.1021/ja103080d
    日期:2010.5.26
    The rhodium(III)-catalyzed hydroarylation of internal alkynes is described. Good yields are obtained for a variety of alkynes, and excellent regioselectivity is observed for unsymmetrically substituted alkynes. The reaction also gives good yields for a range of arenes. Preliminary mechanistic investigations suggest that this reaction proceeds through arene metalation with the cationic rhodium catalyst, which enables challenging intermolecular reactivity.
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