scholarly journals Four - Component Reaction Between Cyanoacetamide, Aryl Aldehydes and Ethyl Acetoacetate with Ammonium Acetate

2012 ◽  
Vol 9 (2) ◽  
pp. 615-620 ◽  
Author(s):  
Marziyeh Khazaei ◽  
Mohammad Anary-Abbasinejad ◽  
Alireza Hassanabadi ◽  
Bahareh Sadeghi

A new and efficient one-pot synthesis of dihydropyridones derivatives by four-component reaction between cyanoacetamide, aryl aldehydes, and ethyl acetoacetate with ammonium acetate using nano ZnO is described. The reaction was performed in ethanol under reflux conditions and afforded good yields of products.


RSC Advances ◽  
2021 ◽  
Vol 11 (18) ◽  
pp. 10497-10511
Author(s):  
Mehraneh Aghaei-Hashjin ◽  
Asieh Yahyazadeh ◽  
Esmayeel Abbaspour-Gilandeh

Polyhydroquinolines were obtained from a sequential four-component reaction between dimedone or 1,3-cyclohexandione, ethyl acetoacetate, or methyl acetoacetate as a β-ketoester, aldehydes, and ammonium acetate, with Mo@GAA-Fe3O4 MNPs as a green nanocatalyst.


2011 ◽  
Vol 76 (11) ◽  
pp. 1307-1315 ◽  
Author(s):  
Behrooz Maleki ◽  
Hafezeh Salehabadi ◽  
Zeinalabedin Sepehr ◽  
Mina Kermanian

A simple and benign protocol has been explored for the preparation of 2,4,6-triarylpyridines by a one-pot reaction between aryl aldehydes, enolizable ketones and ammonium acetate in the presence of N-bromosuccinimide or trichloroisocyanuric acid as green and neutral catalysts. The reactions proceed smoothly at 130 °C under solvent-free conditions to provide 2,4,6-triarylpyridines in good yields.


1968 ◽  
Vol 41 (1) ◽  
pp. 165-167 ◽  
Author(s):  
Akio Sakurai ◽  
Hiroshi Midorikawa

RSC Advances ◽  
2014 ◽  
Vol 4 (40) ◽  
pp. 20932-20939 ◽  
Author(s):  
Zohre Zarnegar ◽  
Javad Safari

Chitosan-coated Fe3O4 nanoparticles (Fe3O4@CS) were prepared simply through in situ co-precipitation of Fe2+ and Fe3+ ions via NH4OH in an aqueous solution of chitosan and their catalytic activity was investigated in the synthesis of 2,4,5-trisubstituted imidazoles by a one-pot condensation of benzil derivatives, aryl aldehydes and ammonium acetate in EtOH.


2013 ◽  
Vol 41 (2) ◽  
pp. 1001-1009 ◽  
Author(s):  
Alimohammad Dehghan ◽  
Sonia Singh ◽  
Mohammad Anary-Abbasinejad ◽  
Alireza Hassanabadi

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Saurabh Puri ◽  
Balbir Kaur ◽  
Anupama Parmar ◽  
Harish Kumar

Copper perchlorate hexahydrate as an efficient catalyst was used for the synthesis of polyhydroquinolines by four-component condensation reaction of aldehyde, ethyl acetoacetate, dimedone, and ammonium acetate in excellent yields and short reaction times at room temperature under ultrasound irradiation. This novel synthetic method is especially favoured because it provides a synergy between copper perchlorate hexahydrate and ultrasound irradiation which offers the advantages of high yields, short reaction times, simplicity, and easy workup compared to the conventional methods reported in the literature.


Author(s):  
Behrooz Maleki ◽  
Reza Tayebee ◽  
Mina Kermanian ◽  
Samaneh Sedigh Ashrafi

Solvent-free, one-pot synthesis of polyhdroquinoline and 1,8-dioxodecahydroacridine derivatives have been described via Hantzsch condensation of various aldehydes, ammonium acetate with (<em>i</em>) cyclic 1,3-dicarbonyl compounds and ethyl acetoacetate and (<em>ii</em>) cyclic 1,3-dicarbonyl compounds (2 mmoles) in a very simple, efficient, and environmentally benign method using 1,3-(dibromo or dichloro)-5,5-dimethylhydantoin as a cheap, non-toxic and neutral catalyst with up to excellent yields.


2013 ◽  
Vol 37 (1) ◽  
pp. 11-13 ◽  
Author(s):  
Bahareh Sadeghi ◽  
Ashraf Namakkoubi ◽  
Alireza Hassanabadi

The solvent-free Hantzsch reaction between ethyl acetoacetate or 1,3-indandione, an aromatic aldehyde and ammonium acetate catalysed by BF3.SiO2 nanoparticles provided an efficient one-step synthesis of 1,4-dihydropyridines in excellent yields.


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