Microwave Irradiation: Synthesis and Characterization of Substituted Pyranoquinolines

2020 ◽  
Vol 17 ◽  
Author(s):  
Maharajan Abirami ◽  
Senniappan Thamarai Selvi ◽  
Vetrivel Nadaraj

: A new series of pyrano[2,3-b]quinolines were synthesized from 3-formylquinolin-2(1H)-ones via Knoevenagel condensation followed by cyclization reaction of ethyl cyanoacetate using DMSO as solvent. This methodology is a simple; clean, fast, efficient, eco-friendly, less reaction time with an improvement in the yield and purity of the product. The structures of newly synthesized compounds were confirmed by IR, NMR, Mass and elemental analysis.

2014 ◽  
Vol 625 ◽  
pp. 213-216 ◽  
Author(s):  
Siti Fatimah Mohamed Razak ◽  
Norzita Ngadi

A novel hybrid flocculant of acrylamide and cellulose was synthesized by using microwave irradiation method. Cellulose was extracted from kenaf by using TAPPI method. 57.4% of percentage grafting and efficiency has been obtained from the grafting process. The hybrid flocculant properties were characterized by using FTIR spectroscopy, FESEM and elemental analysis. Additional peaks that appear in FTIR result, presence of nitrogen in elemental analysis and granular structure of PAM attached in fibrillar structure of cellulose proved that PAM was successfully grafted onto cellulose backbone.


2021 ◽  
Vol 09 ◽  
Author(s):  
Krishnappa B Badiger ◽  
Santosh Y Khatavi ◽  
Prashant B Hiremath ◽  
Kantharaju Kamanna

Background: The present work describes an eco-friendly and sustainable approach for the Knoevenagel condensation of an aromatic aldehyde with ethyl cyanoacetate, and salicylaldehyde with Meldrum acid for the synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin (2-oxo-2H-1-benzopyran) derivatives, respectively. The reaction performed under greener catalytic media Water Extract of Watermelon Fruit Peel Ash (WEWFPA) is an eco-friendly protocol derived from the agro-waste feedstock. Various protocols have been reported for the synthesis of Knoevenagel condensation reaction using a hazardous catalyst or/and solvent found toxic to the environment, reaction time longer, poor yield, and required purification of the final product. The present method provides several added advantages of being completely greener, economic, giving high yield, inexpensive catalyst, and the final product isolated in pure form with good yield. Objective: The objective of the study was to develop a green methodology for the synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives. Results: The agro-waste based catalyst developed avoids the use of external inorganic/organic base, additives, and solvent-free synthesis of Knoevenagel condensation of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives under rt and microwave irradiation, respectively described. The microwave irradiation condition requires less time for the completion of the reaction and also gave better yield isolation Methods: We have demonstrated WEWFPA as a greener homogenous agro-waste is employed under rt stirring and microwave irradiation for the economic synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives. The developed method was found robust, non-hazardous and solvent-free with simple work-up gave target product. Conclusion: In conclusion, we have established an efficient, simple, agro-waste based catalytic approach for the synthesis of ethylbenzylidenecyanoacetate and 3-carboxy coumarin derivatives employing WEWFPA as an efficient catalyst under rt stirring and microwave synthesis, respectively. The method is a greener, economical and eco-friendly approach for the synthesis of Knoevenagel condensation products. The advantages of the present approach are solvent-free, no external metal, chemical base free, short reaction time and isolated product in good to excellent yields. The catalyst is agro-waste derived, which has abundant in natural sources, thus making the present approach a greener one.


2012 ◽  
Vol 262 ◽  
pp. 405-409
Author(s):  
Yang Liu ◽  
Shan Shan Li ◽  
Xin Yan Yang ◽  
Chong Xing Huang

A new-type foam composites were fabricated by baking method from a mixture of cassava starch. A central composite design was constructed using the software Statistics Analysis System 9.0 to evaluate the static compression stress of foamed material. The optimum dosages of adhesive, foaming agent, catalyst were 2.0g, 6.0g, 2.4g, respectively; reaction temperature 65°C; reaction time 16 hour.


2010 ◽  
Vol 16 (1) ◽  
pp. 89-95
Author(s):  
Mihaela Mocanu

The sulfonamidic moiety is much encountered in structures of bioactive compounds. In the present paper the studies on the sulfonamidated aryloxyalkylcarboxylic acids are extended by their attaching on certain substrata able to confer some special biological properties to the final products, such as anti-tumor and antioxidant actions useful in treating inflammatory processes, ulcer, convulsions and diabetes, as well as a herbicidal action. The stepwise syntheses of the sulfonamidated aryloxyalkylcarboxylic acid derivatives and their characterization by elemental analysis data and IR, 1H-NMR and UV-Vis spectral measurements are described. The newly obtained compounds could show potential pharmaceutical and herbicide properties.


2014 ◽  
Vol 11 (2) ◽  
pp. 477-485 ◽  
Author(s):  
Baghdad Science Journal

In this study, chalcones were synthesis by condensing 2-acetylpyridine with aromatic aldehyde derivatives in dilute ethanolic potassium hydroxide solution at room temperature according to Claisen-Schmidt condensation. After that, new heterocyclic derivatives such as Oxazine, Thiazine and Pyrazol were synthesis by reaction between chalcones with urea, thiourea and hydrazine hydrate respectively scheme 1. All these compounds wrer characterization by FTIR, 1H-NMR spectroscopy and elemental analysis.


RSC Advances ◽  
2015 ◽  
Vol 5 (70) ◽  
pp. 56507-56517 ◽  
Author(s):  
R. Sasikala ◽  
S. Kutti Rani ◽  
D. Easwaramoorthy ◽  
K. Karthikeyan

A click and three component A3 coupling reactions were achieved by lanthanum loaded CuO NPs under ultrasonication. 1,4-Disubstituted 1,2,3-triazoles and propargylamines were synthesized in a short reaction time with high regioselectivity and yields.


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