19655-60-8Relevant academic research and scientific papers
Pd-Catalyzed Alkylation of (Iso)quinolines and Arenes: 2-Acylpyridine Compounds as Alkylation Reagents
Wu, Qingsong,Han, Shuaijun,Ren, Xiaoxiao,Lu, Hongtao,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng
supporting information, p. 6345 - 6348 (2018/10/20)
The first Pd-catalyzed alkylation of (iso)quinolines and arenes is reported. The readily available and bench-stable 2-acylpyridine compounds were used as an alkylation reagent to form the structurally versatile alkylated (iso)quinolines and arenes. The method affords a convenient pathway for the introduction of alkyl groups into organic molecules.
Preparation method of quinoline derivative
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Paragraph 0109; 0110, (2017/06/02)
The invention provides a preparation method of a quinoline derivative. The method includes the steps of: in the presence of an oxidizing agent, adding a catalyst, then adding aniline or aromatic amine with different substituents, at the same time adding alcohol for reaction so as to prepare the quinoline derivative by one step. Specifically, the catalyst comprises a metal catalyst, an assistant catalyst I and an assistant catalyst II; the metal catalyst is a transition metal catalyst; the assistant catalyst I is an alkaline nitrogen-containing ligand; and the assistant catalyst II is an acidic compound. The quinoline derivative prepared by the method provided by the invention has stable performance and high purity. And the preparation method of the quinoline derivative can prepare quinoline, 2-methylquinoline, 8-hydroxyquinoline quinoline and other derivatives by one-step reaction, and the preparation method is simple and practicable. The preparation process does not produce new "three wastes", is environment-friendly, and provides a green and environment-friendly synthesis method. The preparation method has the characteristics of few raw material variety, little reaction equipment, few preparation step and low cost, and is more suitable for industrial production.
Assembly of Diversely Substituted Quinolines via Aerobic Oxidative Aromatization from Simple Alcohols and Anilines
Li, Jixing,Zhang, Jinlong,Yang, Huameng,Jiang, Gaoxi
supporting information, p. 3284 - 3290 (2017/03/23)
An aerobic oxidative aromatization of simple aliphatic alcohols and anilines under the Pd(OAc)2/2,4,6-Collidine/Br?nsted acid catalytic system has been established, providing a direct approach for the preparation of diverse substituted quinoline derivatives in high yields with wide functional group tolerance. Practically, the protocol can be easily scaled up to gram-scale and was utilized in the concise formal synthesis of a promising herbicide candidate.
Synthesis of quinolines from glycerol over tungstic acid functionalized mesoporous KIT-6 catalyst in aqueous medium
Udayakumar,Pandurangan
, p. 919 - 928 (2017/08/04)
Mesoporous tungstic acid functionalized KIT-6 has been synthesized through a condensation of (3-chloropropyl) triethoxysilane and Si-KIT-6 followed by substitution of chloromethylation functionalized KIT-6 by sodium tungstate dihydrate. The synthesized tungstic acid functionalized KIT-6 (W-KIT-6) was characterized by low and wide angle X-ray diffraction analysis (XRD), N2 adsorption-desorption isotherm, scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), NH3-temperature programmed desorption (NH3-TPD), 13C CP/MAS NMR spectrum and FT-IR analysis. The functionalized KIT-6 posses surface area of 663 m2/g with corresponding pore size 6.3 nm and pore volume 0.65 cm3/g. The catalytic activity of W-KIT-6 nanoparticles evaluated in the Skraup synthesis of quinoline and its derivatives using water as solvent, the results show the target compound was obtained as 89% yield with complete conversion of glycerol (100%) under the reaction conditions of 200°C for 3 h. The catalyst has been recycled for five times without significant loss in catalytic activity.
