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2-(4-ethoxyphenyl)-5-phenyl-4,5-dihydrooxazole | 1373758-35-0

中文名称
——
中文别名
——
英文名称
2-(4-ethoxyphenyl)-5-phenyl-4,5-dihydrooxazole
英文别名
2-(4-Ethoxyphenyl)-5-phenyl-4,5-dihydro-1,3-oxazole
2-(4-ethoxyphenyl)-5-phenyl-4,5-dihydrooxazole化学式
CAS
1373758-35-0
化学式
C17H17NO2
mdl
——
分子量
267.327
InChiKey
UGRPEJGOZYIUAN-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    30.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    苯乙烯 、 3-(4-ethoxyphenyl)-1,4,2-dioxazol-5-one 在 carbonyl(meso-tetrakis(4-tolyl)porphyrinato)ruthenium(II) 、 、 copper dichloride 作用下, 以 甲苯 为溶剂, 以47%的产率得到2-(4-ethoxyphenyl)-5-phenyl-4,5-dihydrooxazole
    参考文献:
    名称:
    Synthesis of 2,5-Disubstituted Oxazoles and Oxazolines Catalyzed by Ruthenium(II) Porphyrin and Simple Copper Salts
    摘要:
    A novel and moderate synthesis of 2,5-disubstituted oxazoles and oxazolines involving ruthenium(II) porphyrin copper chloride catalyzed cyclization was developed. These reactions using readily available benzene carboxylic acids and phenylethenes or phenylacetylenes are performed under mild conditions. The reactions proceed in series, giving rise to the formation of an intermolecular C-N bond and an intramolecular C-O bond, which yield oxazole or oxazoline derivatives simultaneously.
    DOI:
    10.1021/jo202663n
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文献信息

  • Synthesis of 2,5-Disubstituted Oxazoles and Oxazolines Catalyzed by Ruthenium(II) Porphyrin and Simple Copper Salts
    作者:Chuan Long Zhong、Bo Yang Tang、Ping Yin、Yue Chen、Ling He
    DOI:10.1021/jo202663n
    日期:2012.5.4
    A novel and moderate synthesis of 2,5-disubstituted oxazoles and oxazolines involving ruthenium(II) porphyrin copper chloride catalyzed cyclization was developed. These reactions using readily available benzene carboxylic acids and phenylethenes or phenylacetylenes are performed under mild conditions. The reactions proceed in series, giving rise to the formation of an intermolecular C-N bond and an intramolecular C-O bond, which yield oxazole or oxazoline derivatives simultaneously.
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