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1-(2,5-dimethyl-1,4-diphenyl-1H-pyrrol-3-yl)ethanone | 1168152-71-3

中文名称
——
中文别名
——
英文名称
1-(2,5-dimethyl-1,4-diphenyl-1H-pyrrol-3-yl)ethanone
英文别名
1-(2,5-dimethyl-1,4-diphenyl-1H-pyrrol-3-yl)ethan-1-one
1-(2,5-dimethyl-1,4-diphenyl-1H-pyrrol-3-yl)ethanone化学式
CAS
1168152-71-3
化学式
C20H19NO
mdl
——
分子量
289.377
InChiKey
ZDZZMYBELKZDIY-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):
    4.96
  • 重原子数:
    22.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    22.0
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    苯硼酸 在 copper(II) oxide 作用下, 以 为溶剂, 反应 6.0h, 生成 1-(2,5-dimethyl-1,4-diphenyl-1H-pyrrol-3-yl)ethanone
    参考文献:
    名称:
    铜催化 α-酮醛、1,3-二羰基化合物和有机硼酸在水中的三组分反应:制备 1,4-二酮的途径
    摘要:
    已开发出一种新型的 α-酮醛、1,3-二羰基化合物和有机硼酸在水中由 CuO 催化的三组分反应,可得到多种含有 1,3/1,4-二酮的产物。该方法具有原料易得、底物范围广、收率高、克级合成、反应条件温和等优点。
    DOI:
    10.1021/acs.joc.1c01100
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文献信息

  • Indium(III) Chloride-Catalyzed Propargylation/Amination/Cycloisomerization Tandem Reaction: One-Pot Synthesis of Highly Substituted Pyrroles from Propargylic Alcohols, 1,3-Dicarbonyl Compounds and Primary Amines
    作者:Xiao-tao Liu、Lei Huang、Fei-jian Zheng、Zhuang-ping Zhan
    DOI:10.1002/adsc.200800473
    日期:——
    propargylation/amination/cycloisomerization tandem process has been developed for the synthesis of highly substituted pyrroles derivatives from propargylic alcohols, 1,3-dicarbonyl compounds and primary amines using indium(III) chloride as a multifunctional catalyst. This method provides a flexible and rapid route to substituted pyrroles.
    已经开发了一种方便的一锅法炔丙基化/胺化/环异构化串联方法,该方法用于使用氯化铟(III)作为多功能催化剂,从炔丙醇,1,3-二羰基化合物和伯胺合成高度取代的吡咯生物。这种方法为取代吡咯提供了一种灵活而快速的途径。
  • Nano CoFe<sub>2</sub>O<sub>4</sub> supported antimony(<scp>iii</scp>) as an efficient and recyclable catalyst for one-pot three-component synthesis of multisubstituted pyrroles
    作者:Bao-Le Li、Hai-Chuan Hu、Li-Ping Mo、Zhan-Hui Zhang
    DOI:10.1039/c3ra47855f
    日期:——
    A novel magnetic nano-CoFe2O4 supported Sb ([CoFe2O4@SiO2–DABCO–Sb]) was successfully constructed, which exhibited high catalytic activity for one-pot three-component synthesis of multisubstituted pyrroles in the reaction of amines, nitroolefin and 1,3-dicarbonyl compounds. The magnetic heterogeneous catalyst could be easily recovered using an external magnet and reused many times without significant
    成功地构建了一种新型的磁性纳米CoFe 2 O 4负载的Sb([CoFe 2 O 4 @SiO 2 –DABCO-Sb]),该催化剂对多取代吡咯的一锅三组分合成具有很高的催化活性。胺,硝基烯烃和1,3-二羰基化合物。磁性非均相催化剂可以使用外部磁体容易地回收,并且可以多次重复使用而不会显着降低催化活性。
  • Natural Hydroxyapatite: Green Catalyst for the Synthesis of Pyrroles, Inhibitors of Corrosion
    作者:Abdelhadi Louroubi、Abdallah Nayad、Ali Hasnaoui、Rachid Idouhli、Abdessalam Abouelfida、Larbi El Firdoussi、Mustapha Ait Ali
    DOI:10.1155/2021/6613243
    日期:2021.3.5

    Polysubstituted pyrroles have been synthesized in good yields via a four-component one-pot reaction of 1,3-dicarbonyl compounds, amines, aldehydes, and nitroalkanes using natural hydroxyapatite (HAp) as an efficient green catalyst. This strategy provides advantages such as simple experimental and work-up procedures, mild conditions, high selectivity, low cost, high atom economy, and environmental friendliness; it uses a green commercial catalyst and does not require a solvent. The electrochemical behavior of S300 steel in 1 M hydrochloric acidic was studied in the presence of these heterocyclic compounds. The results showed good inhibition efficiency for steel in acidic media.

    通过使用天然羟基磷灰石(HAp)作为高效的绿色催化剂,通过1,3-二酮化合物、胺、醛和硝基烷烃的四组分一锅法反应,合成了多取代吡咯化合物,产率良好。这种策略具有简单的实验和操作程序、温和的条件、高选择性、低成本、高原子经济性和环保友好等优点;它使用了一种绿色的商业催化剂,无需溶剂。在1M盐酸存在下,研究了这些杂环化合物对S300钢在酸性介质中的电化学行为。结果显示这些化合物对酸性介质中的钢具有良好的抑制效果。
  • An efficient synthesis of highly substituted functionalized pyrroles via a four-component coupling reaction catalyzed by Fe(III)-Schiff base/SBA-15
    作者:Ghasem Rezanejade Bardajee、Aseyeh Ghaedi、Hamideh Hazrati、Farnaz Jafarpour
    DOI:10.1080/24701556.2020.1744650
    日期:2020.12.1
    Abstract An environmentally friendly, straightforward, and cheap synthesis of highly substituted functionalized pyrrole derivatives via one pot four-component reactions of 1,3-dicarbonyl compounds, amines, aromatic aldehydes, and nitroalkanes have been developed. This methodology provides desired pyrroles in good-to-excellent yields in the presence of Fe (III)-Schiff base/SBA-15 as a heterogeneous
    摘要 通过1,3-二羰基化合物,胺,芳族醛和硝基烷的一锅四组分反应,已经开发了一种环境友好,直接且廉价的高取代官能化吡咯生物的合成方法。该方法在Fe(III)-席夫碱/ SBA-15作为非均相催化剂存在下,以良好至优异的产率提供了所需的吡咯
  • Modular CeCl3·7H2O-catalyzed multi-component synthesis of 1,2,3,4-tetrasubstituted pyrroles under microwave irradiation and their further trichloroisocyanuric acid-mediated conversion into 5-sulfenylpyrrole derivatives
    作者:Claudio C. Silveira、Samuel R. Mendes、Guilherme M. Martins、Sheila C. Schlösser、Teodoro S. Kaufman
    DOI:10.1016/j.tet.2013.08.035
    日期:2013.10
    A modular, multicomponent synthesis of 1,2,3,4-tetrasubstituted pyrroles promoted by the inexpensive CeCl3 center dot 7H(2)O, is reported. The reaction was carried out under microwave irradiation, affording good yields of products in short time. Scope and limitations were explored and a plausible reaction mechanism is discussed. The resulting heterocycles were smoothly and efficiently converted into their corresponding 5-arylsulfenyl derivatives by reaction with diaryl disulfides and trichloroisocyanuric acid in EtOAc. (C) 2013 Elsevier Ltd. All rights reserved.
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