Aiding the versatility of simple ammonium ionic liquid by the synthesis of bioactive 1,2,3,4-tetrahydropyrimidine, 2-aminothiazole and quinazolinones derivatives.

2021 ◽  
Author(s):  
Satish Kumar Awasthi ◽  
Praachi Kakati ◽  
Preeti Singh ◽  
PRIYANKA YADAV

Simple ammonium ionic liquids [ILs] are the efficient, green, environment friendly catalyst in promoting Biginelli condensation reaction, Hantzsch reaction and Niementowski reaction to afford 1,2,3,4-tetrahydropyrimidine, 2-aminothiazole and quinazolinone derivatives respectively...

2011 ◽  
Vol 332-334 ◽  
pp. 1884-1887
Author(s):  
Fang Yang ◽  
Hong Jun Zang ◽  
Qing Kai Wang ◽  
Bo Wen Cheng ◽  
Yuan Lin Ren ◽  
...  

A simple and efficient one-pot method for the preparation of 2H-indazolo [2,1-b] phthalazine-triones from phthalhydrazide, dimedone and aromatic aldehydes has been developed using ionic liquids as catalysts. Two ionic liquid catalysts are described, and the ionic liquid [(CH2)4SO3HMIM]HSO4 catalyst is found to be more effective than [HMIM]HSO4 for this condensation reaction.


RSC Advances ◽  
2016 ◽  
Vol 6 (47) ◽  
pp. 41108-41113 ◽  
Author(s):  
Hongyan Zhao ◽  
Guijie Mao ◽  
Huatao Han ◽  
Jinyi Song ◽  
Yang Liu ◽  
...  

Cu NPs@RGO can effectively catalyze Ullmann C–C homocoupling of aryl halides and arylboronic acids under microwave irradiation in green solvent ionic liquid..


2018 ◽  
Vol 21 (1) ◽  
pp. 14-18
Author(s):  
Ashraf S. Shahvelayati ◽  
Maryam Ghazvini ◽  
Khadijeh Yadollahzadeh ◽  
Akram S. Delbari

Background: The development of multicomponent reactions (MCRs) in the presence of task-specific ionic liquids (ILs), used not only as environmentally benign reaction media, but also as catalysts, is a new approach that meet with the requirements of sustainable chemistry. In recent years, the use of ionic liquids as a green media for organic synthesis has become a chief study area. This is due to their unique properties such as non-volatility, non-flammability, chemical and thermal stability, immiscibility with both organic compounds and water and recyclability. Ionic liquids are used as environmentally friendly solvents instead of hazardous organic solvents. Objective: We report the condensation reaction between α-oximinoketone and dialkyl acetylene dicarboxylate in the presence of triphenylphosphine to afford substituted pyrroles under ionic liquid conditions in good yields. Result: Densely functionalized pyrroles was easily prepared from reaction of α-oximinoketones, dialkyl acetylene dicarboxylate in the presence of triphenylphosphine in a quantitative yield under ionic liquid conditions at room temperature. Conclusion: In conclusion, ionic liquids are indicated as a useful and novel reaction medium for the selective synthesis of functionalized pyrroles. This reaction medium can replace the use of hazardous organic solvents. Easy work-up, synthesis of polyfunctional compounds, decreased reaction time, having easily available-recyclable ionic liquids, and good to high yields are advantages of present method.


2014 ◽  
Vol 52 (1-2) ◽  
pp. 41-48
Author(s):  
L. Anteina ◽  
A. Gaidule ◽  
A. Zicmanis

Abstract We report the preparation, characterization and exploitation of 1,3-dialkylimidazolium dimethyl phosphates. Condensation reactions of benzaldehyde with ethyl cyanoacetate and with malonic acid were performed in these ionic liquids either in absence or in presence of other catalysts. The effect of ionic liquid structure on the condensation reaction rates and yields was discussed


2020 ◽  
Vol 1 (2) ◽  
pp. 138-153
Author(s):  
Lisa Mullins ◽  
James A. Sullivan

Two catalysts are prepared by tethering ionic liquid cation components (1-(propyl-3-sulfonate)-3-(3-trimethoxysilylpropyl) imidazolium) with either chloride or sulphate anions, to the surface of a mesoporous SiO2 material through a condensation reaction. These are characterized using elemental analysis, TGA-MS, FTIR (and D-FTIR), TEM, physisorption and NH3 adsorption (TPD and FTIR), and applied in the valeric acid + pentanol esterification reaction to form the sustainable biodiesel Pentyl Valerate. The material containing the sulfate counter-ion was significantly more active than the chloride analogue.


2014 ◽  
Vol 6 (12) ◽  
pp. 4067-4076 ◽  
Author(s):  
Jing Chen ◽  
Yuzhi Wang ◽  
Qun Zeng ◽  
Xueqin Ding ◽  
Yanhua Huang

A series of hydroxyl ammonium ionic liquids have been designed and synthesized and used for the extraction of proteins.


RSC Advances ◽  
2017 ◽  
Vol 7 (6) ◽  
pp. 3214-3221 ◽  
Author(s):  
R. C. M. Alves Sobrinho ◽  
P. M. de Oliveira ◽  
C. R. Montes D'Oca ◽  
D. Russowsky ◽  
M. G. Montes D'Oca

In this work, an efficient and reusable pyrrolidinium ionic liquid (PyrrIL) catalysis system was developed and used in a Knoevenagel condensation reaction of long-chain aldehydes with several 1,3-dicarbonyl compounds.


2021 ◽  
Vol 25 ◽  
Author(s):  
Parmita Phukan ◽  
Diganta Sarma

: The use of natural and environment friendly energy sources for betterment of the living society has become an active concern in both government and public sector. Due to this, responsible use of global resources has become a growing concern among people. Similarly, in chemical industry especially in pharmaceutical fields, there is constant pressure in reducing hazardous organic solvents and environmentally detrimental laboratory materials. The use of ionic liquids in efficient synthesis of a wide array of fundamentally important structural motifs has gained tremendous importance in the scientific era. In this review, synthesis of two such medicinally relevant moieties, namely, triazole and pyrazole, in green and sustainable ionic liquid have been discussed.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Firouzeh Nemati ◽  
Sara G. Alizadeh

A simple and efficient method for the one-pot Biginelli condensation reaction of aldehydes,β-dicarbonyl compounds, and urea or thiourea employing [DABCO](SO3H)2Cl2as a novel ionic liquid catalyst is described.


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