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1-[4-(5-methanesulfonylthiophene-2-yl)-phenyl]ethanone | 1313758-52-9

中文名称
——
中文别名
——
英文名称
1-[4-(5-methanesulfonylthiophene-2-yl)-phenyl]ethanone
英文别名
1-[4-(5-Methylsulfonylthiophen-2-yl)phenyl]ethanone
1-[4-(5-methanesulfonylthiophene-2-yl)-phenyl]ethanone化学式
CAS
1313758-52-9
化学式
C13H12O3S2
mdl
——
分子量
280.368
InChiKey
QSYLRXPAKVKARF-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):
    2.5
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    87.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-甲基磺酰噻吩4-溴苯乙酮potassium acetate 、 palladium diacetate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 16.0h, 以73%的产率得到1-[4-(5-methanesulfonylthiophene-2-yl)-phenyl]ethanone
    参考文献:
    名称:
    Palladium-Catalyzed Direct Arylation of Thiophenes Bearing SO2R Substituents
    摘要:
    The palladium-catalyzed direct arylation of SO2R-substituted thiophene derivatives was found to proceed regioselectively at CS and in high yields using a variety of aryl bromides and as low as 0.5-0.1 mol % of phosphine-free Pd(OAc)(2) as the catalyst. For these reactions, sulfonyls, sulfonamides, or even a sulfonic ester as the thiophene substituents were successfully employed.
    DOI:
    10.1021/jo200918n
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文献信息

  • Palladium-Catalyzed Direct Arylation of Thiophenes Bearing SO<sub>2</sub>R Substituents
    作者:Charles Beromeo Bheeter、Jitendra K. Bera、Henri Doucet
    DOI:10.1021/jo200918n
    日期:2011.8.5
    The palladium-catalyzed direct arylation of SO2R-substituted thiophene derivatives was found to proceed regioselectively at CS and in high yields using a variety of aryl bromides and as low as 0.5-0.1 mol % of phosphine-free Pd(OAc)(2) as the catalyst. For these reactions, sulfonyls, sulfonamides, or even a sulfonic ester as the thiophene substituents were successfully employed.
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