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3-methyl-1,3-diphenyl-3,4-dihydrobenzo[f]quinoline

中文名称
——
中文别名
——
英文名称
3-methyl-1,3-diphenyl-3,4-dihydrobenzo[f]quinoline
英文别名
3-methyl-1,3-diphenyl-4H-benzo[f]quinoline
3-methyl-1,3-diphenyl-3,4-dihydrobenzo[f]quinoline化学式
CAS
——
化学式
C26H21N
mdl
——
分子量
347.459
InChiKey
FNIAGYOBBZZGRM-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):
    6.6
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    苯乙炔2-萘胺 在 indium(III) triflate 作用下, 以 甲苯 为溶剂, 反应 10.0h, 以85%的产率得到3-methyl-1,3-diphenyl-3,4-dihydrobenzo[f]quinoline
    参考文献:
    名称:
    Indium(III)-Catalyzed Tandem Hydroamination–Hydroarylation of Naphthylamines with Phenylacetylenes
    摘要:
    A one-pot, three-component method for the synthesis of benzo-fused quinolines has been developed by tandem reaction between phenylacetylenes and naphthylamines. The first step of the reaction is hydroamination of the alkyne followed by a hydroarylation reaction to form the quinolines. Indium(III) trifluoromethanesulfonate was shown to be an efficient catalyst for the transformations, and the reaction proceeded in the absence of any other co-catalyst or additive to give the corresponding quinolines in good to excellent yields.
    DOI:
    10.1055/s-0033-1341234
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文献信息

  • Indium(III)-Catalyzed Tandem Hydroamination–Hydroarylation of Naphthylamines with Phenylacetylenes
    作者:Dipak Prajapati、Nimmakuri Rajesh、Rupam Sarma
    DOI:10.1055/s-0033-1341234
    日期:——
    A one-pot, three-component method for the synthesis of benzo-fused quinolines has been developed by tandem reaction between phenylacetylenes and naphthylamines. The first step of the reaction is hydroamination of the alkyne followed by a hydroarylation reaction to form the quinolines. Indium(III) trifluoromethanesulfonate was shown to be an efficient catalyst for the transformations, and the reaction proceeded in the absence of any other co-catalyst or additive to give the corresponding quinolines in good to excellent yields.
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