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1-benzyl-3-methyl-2-phenyl-1H-pyrrole

中文名称
——
中文别名
——
英文名称
1-benzyl-3-methyl-2-phenyl-1H-pyrrole
英文别名
1-Benzyl-3-methyl-2-phenylpyrrole
1-benzyl-3-methyl-2-phenyl-1H-pyrrole化学式
CAS
——
化学式
C18H17N
mdl
——
分子量
247.34
InChiKey
QLKVXONXMIIYPO-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):
    4.3
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    4.9
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    2-(二苄基氨基)乙醛 氢气lithium diisopropyl amide 作用下, 以 四氢呋喃甲醇 为溶剂, -78.0 ℃ 、101.33 kPa 条件下, 生成 1-benzyl-3-methyl-2-phenyl-1H-pyrrole
    参考文献:
    名称:
    A versatile synthesis of polysubstituted pyrroles
    摘要:
    The aldol products formed by the reaction between alpha-(N-benzyl or N-Cbz)amino aldehydes and lithium enolates of various ketones, were subjected to hydrogenolysis to give polysubstituted pyrroles in good yields (50-91%). The scope and limitations of this methodology are explored. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)01203-5
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文献信息

  • Multicomponent reactions in PEG-400: ruthenium-catalyzed synthesis of substituted pyrroles
    作者:Srivari Chandrasekhar、Vidyavathi Patro、Lahu N. Chavan、Rambabu Chegondi、René Grée
    DOI:10.1016/j.tetlet.2014.08.105
    日期:2014.10
    An efficient and eco-friendly method for the synthesis of substituted pyrroles has been developed via ruthenium-catalyzed multicomponent reaction of ketone, amine, and ethylene glycol in PEG-400 as solvent medium without using any external ligand. The catalytic system and solvent can be recycled with the same, as well as different, ketones with minimum loss of Ru-catalyst activity.
    通过在不使用任何外部配体的情况下,通过钌催化的PEG-400中的酮,胺和乙二醇的多组分反应,开发了一种高效,环保的取代吡咯合成方法。催化体系和溶剂可以用相同或不同的酮循环使用,而Ru催化剂的活性损失最小。
  • A versatile synthesis of polysubstituted pyrroles
    作者:Bharat Lagu、Meng Pan、Michael P Wachter
    DOI:10.1016/s0040-4039(01)01203-5
    日期:2001.8
    The aldol products formed by the reaction between alpha-(N-benzyl or N-Cbz)amino aldehydes and lithium enolates of various ketones, were subjected to hydrogenolysis to give polysubstituted pyrroles in good yields (50-91%). The scope and limitations of this methodology are explored. (C) 2001 Elsevier Science Ltd. All rights reserved.
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