ChemInform Abstract: Design of 1-Methylimidazolium Tricyanomethanide as the First Nanostructured Molten Salt and Its Catalytic Application in the Condensation Reaction of Various Aromatic Aldehydes, Amides and β-Naphthol Compared with Tin Dioxide Nanopart

ChemInform ◽  
2015 ◽  
Vol 46 (41) ◽  
pp. no-no
Author(s):  
Mohammad Ali Zolfigol ◽  
Saeed Baghery ◽  
Ahmad Reza Moosavi-Zare ◽  
Seyed Mohammad Vahdat ◽  
Heshmatollah Alinezhad ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (56) ◽  
pp. 45027-45037 ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Saeed Baghery ◽  
Ahmad Reza Moosavi-Zare ◽  
Seyed Mohammad Vahdat ◽  
Heshmatollah Alinezhad ◽  
...  

1-Methyl imidazolium tricyanomethanide {[HMIM]C(CN)3} as a novel nano molten salt (MS) was synthesized and applied for the synthesis of 1-amidoalkyl-2-naphthols and compared with tin dioxide (SnO2) nanoparticles.


2018 ◽  
Vol 21 (4) ◽  
pp. 298-301 ◽  
Author(s):  
Ghasem Marandi

Aim and Objective: The reaction of cyclohexylisocyanide and 2-aminopyridine-3- carboxylic acid in the presence of benzaldehyde derivatives in ethanol led to 3-(cyclohexylamino)-2- arylimidazo[1,2-a]pyridine-8-carboxylic acids in high yields. In a three component condensation reaction, isocyanide reacts with 2-aminopyridine-3-carboxylic acid and aromatic aldehydes without any prior activation. Material and Methods: The synthesized products have stable structures which have been characterized by IR, 1H, 13C and Mass spectroscopy as well as CHN-O analysis. Results: In continuation of our attempts to develop simple one-pot routes for the synthesis of 3- (cyclohexylamino)-2-arylimidazo[1,2-a]pyridine-8-carboxylic acids, aromatic aldehydes with divers substituted show a high performance. Conclusion: In conclusion, this study introduces the art of combinatorial chemistry using a simple one-pot procedure for the synthesis of new materials which are interesting compounds in medicinal and biological sciences.


2020 ◽  
Vol 14 ◽  
Author(s):  
Soufiane Akhramez ◽  
Youness Achour ◽  
Mustapha Diba ◽  
Lahoucine Bahsis ◽  
Hajiba Ouchetto ◽  
...  

Background: In this study, an efficient synthesis of novel bispyrazole heterocyclic molecules by condensation of substituted aromatic aldehydes with 1,3-diketo-N-phenylpyrazole by using Mg/Al-LDH as heterogeneous catalyst is reported. The attractive features of this protocol are as follows: mild reaction conditions, good yields and easiness of the catalyst separation from the reaction mixture. Further, a mechanistic study has been performed by using DFT calculations to explain the observed selectivity of the condensation reaction between aryl aldehyde and 1,3-diketo-N-phenylpyrazole via Knoevenagel reaction. The local electrophilicity/ nucleophilicity that allows explaining correctly the experimental finding. Methods: The bispyrazole derivatives 3a-m were prepared by condensation reaction of substituted aromatic aldehydes with 1,3-diketo-Nphenylpyrazole by using Mg/Al-LDH as heterogeneous catalyst under THF solvent at the refluxing temperature. Objective: To synthesize a novel bispyrazole heterocyclic molecule may be have important biological activities and thus can be good candidates for pharmaceutical applications. Results: This protocol describes the Synthesis of Bioactive Compounds under mild reaction conditions, good yields and easiness of the catalyst separation from the reaction mixture. Further, a mechanistic study has been performed by using DFT calculations to explain the observed selectivity of the condensation reaction between aryl aldehyde and 1,3-diketo-N-phenylpyrazole via Knoevenagel reaction. The local electrophilicity/ nucleophilicity that allows explaining correctly the experimental finding. Conclusion: In summary, the pharmacologically interesting bis-pyrazole derivatives have been synthesized through Mg/Al-LDH as a solid base catalyst, in THF as solvent. Thus, the synthesized bioactive compounds containing the pyrazole ring may be have important biological activities and thus can be good candidates for pharmaceutical applications. Therefore, the catalyst Mg/Al-LDH showed high catalytic activity. Besides, a series of bispyrazole molecules were synthesized with a good yield and easy separation of the catalyst by simple filtration. Moreover, DFT calculations and reactivity indexes are used to explain the selectivity of the condensation reaction between aryl benzaldehyde and 1,3-diketo-Nphenylpyrazole via Knoevenagel reaction, and the results are in good agreement with the experimental finding.


2021 ◽  
Vol 25 (11) ◽  
pp. 38-40
Author(s):  
S.R. Jagtap ◽  
R.P. Yadav ◽  
B.B. Bahule ◽  
D.J. Chaudhari

In this study, we are reporting a solvent free Biginelli reaction using aromatic aldehydes, ethyl acetoacetate and urea in presence of cetyl tri-methyl ammonium bromide as a catalyst. The reaction is green and environmentally benign. The yield of three component condensation reaction is excellent. The products were screened for anti-bacterial and anti-fungal activity. The method is simple and convenient. The catalyst is novel and easily available, non-expensive and nontoxic.


2013 ◽  
Vol 1 ◽  
pp. 194308921350716 ◽  
Author(s):  
Elaheh Mosaddegh ◽  
Asadollah Hassankhani ◽  
Sadegh Pourahmadi ◽  
Dadkhoda Ghazanfari

Ball mill–assisted preparation of nano-bio Calcite (CaCO3) based on avian shell and its application as a novel, biodegradable, and heterogeneous catalyst with high catalytic activity and reusability in the green and high efficient synthesis of pyrano[4,3- b]pyrans via a condensation reaction of different aromatic aldehydes, malononitrile, and 4-hydroxy-6-methyl-2 H-pyran-2-one at 120°C under solvent-free conditions is reported. The reaction proceeds to completion within 5–30 min in 90–98% yield. The nanocatalyst was characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), scanning electron microscope (SEM), elemental analysis, and laser particle sizer.


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.


ChemInform ◽  
2010 ◽  
Vol 23 (15) ◽  
pp. no-no
Author(s):  
S. SELVARAJ ◽  
A. DHANABALAN ◽  
A. MERCYPUSHPHALATHA ◽  
N. ARUMUGAM

2017 ◽  
Vol 10 (9) ◽  
pp. 3197-3202 ◽  
Author(s):  
Davood Azarifar ◽  
Younes Abbasi ◽  
Omolbanin Badalkhani

Leucine, a naturally occurring α-amino acid, has been found as an effective catalyst to effect the one-pot three-component condensation reaction between aromatic aldehydes, malononitrile and 5,5-dimethyl-1,3-cyclohexanedione (dimedone). Various 2-amino-4-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile derivatives are conveniently prepared by these reactions in excellent yields. High yields, short reaction times, simple work-up, use of green and naturally occurring catalyst and solvent are the main merits of the present protocol. 


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