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7-heptyl-6-methyl-3-methylene-2-phenyl-2H-furo[3,2-c]pyran-4(3H)-one | 1422048-25-6

中文名称
——
中文别名
——
英文名称
7-heptyl-6-methyl-3-methylene-2-phenyl-2H-furo[3,2-c]pyran-4(3H)-one
英文别名
7-Heptyl-6-methyl-3-methylidene-2-phenylfuro[3,2-c]pyran-4-one;7-heptyl-6-methyl-3-methylidene-2-phenylfuro[3,2-c]pyran-4-one
7-heptyl-6-methyl-3-methylene-2-phenyl-2H-furo[3,2-c]pyran-4(3H)-one化学式
CAS
1422048-25-6
化学式
C22H26O3
mdl
——
分子量
338.447
InChiKey
XJCJKMSNOQTFBE-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:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    methyl 1-phenylprop-2-ynyl carbonate 、 5-heptyl-4-hydroxy-6-methyl-2-pyrone 在 tris(dibenzylideneacetone)dipalladium(0) chloroform complex1,1'-双(二苯基膦)二茂铁 作用下, 以 N-甲基吡咯烷酮 为溶剂, 以64%的产率得到7-heptyl-6-methyl-3-methylene-2-phenyl-2H-furo[3,2-c]pyran-4(3H)-one
    参考文献:
    名称:
    Regiocontrolled Construction of Furo[3,2-c]pyran-4-one Derivatives by Palladium-Catalyzed Cyclization of Propargylic Carbonates with 4-Hydroxy-2-pyrones
    摘要:
    The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively synthesized, respectively.
    DOI:
    10.1021/jo3027092
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文献信息

  • Regiocontrolled Construction of Furo[3,2-<i>c</i>]pyran-4-one Derivatives by Palladium-Catalyzed Cyclization of Propargylic Carbonates with 4-Hydroxy-2-pyrones
    作者:Masahiro Yoshida、Tomomi Nakagawa、Kouki Kinoshita、Kozo Shishido
    DOI:10.1021/jo3027092
    日期:2013.2.15
    The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively synthesized, respectively.
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