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1-(4,5-Dimethyl-3-phenylfuran-2-yl)-1-ethanone | 145663-30-5

中文名称
——
中文别名
——
英文名称
1-(4,5-Dimethyl-3-phenylfuran-2-yl)-1-ethanone
英文别名
1-(4,5-Dimethyl-3-phenylfuran-2-yl)ethanone
1-(4,5-Dimethyl-3-phenylfuran-2-yl)-1-ethanone化学式
CAS
145663-30-5
化学式
C14H14O2
mdl
——
分子量
214.264
InChiKey
VZFAWKLLYKENFL-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):
    3.4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 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:
    4-Phenyl-2,3,6-trimethylpyrylium perchlorate 在 sodium dihydrogenphosphate双氧水sodium acetate 作用下, 以 为溶剂, 反应 0.33h, 以3%的产率得到1-(4,5-Dimethyl-3-phenylfuran-2-yl)-1-ethanone
    参考文献:
    名称:
    Hydrogen peroxide oxidation of polysubstituted pyrylium salts: formation of enol esters and furans
    摘要:
    2,4,6-Trialkylsubstituted pyrylium salts 1 have been known lo afford 2-acyl-3,5-dialkyl-furans 2 in moderate yields (30 - 45%). Oxidation of these salts in buffer solutions (pH = 3 - 4.5) increased the yields of acylfurans to 75%. In contrast, tetra- and penta-substituted pyrylium salts are mainly converted into enol esters with a delta-keto group and furans all originating presumably by C-O bond cleavages in a common intermediate. This intermediate may result by a C-O acyl shift as inferred from analogous compounds with deuterium labelling.
    DOI:
    10.1016/s0040-4020(01)92277-x
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文献信息

  • Hydrogen peroxide oxidation of polysubstituted pyrylium salts: formation of enol esters and furans
    作者:Teodor Silviu Balaban、Monika Hiegemann
    DOI:10.1016/s0040-4020(01)92277-x
    日期:1992.11
    2,4,6-Trialkylsubstituted pyrylium salts 1 have been known lo afford 2-acyl-3,5-dialkyl-furans 2 in moderate yields (30 - 45%). Oxidation of these salts in buffer solutions (pH = 3 - 4.5) increased the yields of acylfurans to 75%. In contrast, tetra- and penta-substituted pyrylium salts are mainly converted into enol esters with a delta-keto group and furans all originating presumably by C-O bond cleavages in a common intermediate. This intermediate may result by a C-O acyl shift as inferred from analogous compounds with deuterium labelling.
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