p-Toluene sulfonic acid-catalysed microwave synthesis of symmetrical bisamides by reaction between aromatic aldehydes and amides

2010 ◽  
Vol 34 (8) ◽  
pp. 478-480 ◽  
Author(s):  
Mohammad Anary-Abbasinejad ◽  
Alireza Hassanabadi ◽  
Motahareh Heidari-Barfeh
Keyword(s):  
Microwave Synthesis ◽  
Sulfonic Acid ◽  
Aromatic Aldehydes ◽  
Toluene Sulfonic Acid

Synthesis of 4-aryl-7-methyl-3,4-dihydropyrano[3,4-e][1,3]oxazine-2,5-dione in Aqueous Media

2016 ◽  
Vol 40 (12) ◽  
pp. 727-728 ◽  
Author(s):  
Allahbakhsh Abdollahi–Irandegan ◽  
Alireza Hassanabadi
Keyword(s):  
Organic Solvents ◽  
Sulfonic Acid ◽  
Present Method ◽  
Aqueous Media ◽  
Aromatic Aldehydes ◽  
Ring Formation ◽  
Green Process ◽  
Toluene Sulfonic Acid ◽  
Oxazine Ring ◽  
Novel Method

A novel method for oxazine ring formation is established using the reaction of 4-hydroxy-6-methyl-2H-pyran-2-one and aromatic aldehydes with methyl carbamate in the presence of p-toluene sulfonic acid (p-TSA) in aqueous media to afford 4-aryl-7-methyl-3,4-dihydropyrano[3,4-e][1,3]oxazine-2,5-dione in excellent yields. The present method does not involve any hazardous organic solvents and could therefore be considered a green process.

scholarly journals Bicyclic [1,3,4]Thiadiazolo[3,2-α]Pyrimidine Analogues: Novel One-Pot Three-Component Synthesis, Antimicrobial, and Antioxidant Evaluation

2021 ◽  
Vol 11 (5) ◽  
pp. 12925-12936
Keyword(s):  
Spectral Data ◽  
Elemental Analysis ◽  
Sulfonic Acid ◽  
Aromatic Aldehydes ◽  
One Pot ◽  
Antibacterial And Antifungal Activities ◽  
Toluene Sulfonic Acid ◽  
Antioxidant Evaluation ◽  
Pyrimidine Analogues ◽  
Antibacterial And Antifungal

A novel one-pot three-component synthesis of 1-(7-methyl-2,5-diphenyl-5H-[1,3,4]thiadiazolo(3,2-α)pyrimidine-6-yl)ethanone (4a-i) derivatives via cyclo-condensation of substituted 2-amino-[1,3,4]thiadiazole (1a-c), acetylacetone (2) and various aromatic aldehydes (3a-c) in the presence of p-toluene sulfonic acid (PTSA) in acetonitrile. Spectral data and elemental analysis have characterized the newly synthesized compounds. The new analogs were screened for their antibacterial and antifungal activities. The majority of the tested compounds displayed significant to moderate efficacy against most of the designated organisms. Among the tested compounds, 4b, 4e, and 4h showed noteworthy efficacy against selected microbes, and compounds 4c and 4i were found to be exceptionally efficient against selected fungal strains. Compound 4c, 4e, 4f, 4i were also designated as best antioxidants against NOx.

scholarly journals Deep eutectic solvents (DESs) as powerful and recyclable catalysts and solvents for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones

2019 ◽  
Vol 8 (1) ◽  
pp. 568-576 ◽  
Author(s):  
Yingna Cui ◽  
Changping Li ◽  
Ming Bao
Keyword(s):  
Catalytic Activity ◽  
Sulfonic Acid ◽  
Choline Chloride ◽  
Catalytic Efficiency ◽  
Aromatic Aldehydes ◽  
Deep Eutectic Solvents ◽  
Green Catalyst ◽  
Toluene Sulfonic Acid ◽  
Recyclable Catalysts ◽  
Main Factor

Abstract Deep eutectic solvents (DESs) are successfully used as powerful and recyclable catalysts and solvents for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones (DHPMs). The acidity of DESs is the main factor that determines catalytic activity. DESs, based on p-toluene sulfonic acid (PTSA) and choline chloride (ChCl), exhibits the highest catalytic activity. ChCl/2PTSA is suitable for a vast variety of aromatic aldehydes with electron-donating and electron-withdrawing groups, different β-diketonates, and urea or thiourea to obtain the corresponding DHPMs. Furthermore, DESs can be recycled easily after synthesis. The reused DESs achieve catalytic efficiency six times without significant changes. This study will provide a new green catalyst and efficient process for the synthesis of DHPMs.

Design, Synthesis, Antimicrobial Evaluation and Molecular Modeling Study of New 2-mercaptoimidazoles (Series-III)

2019 ◽  
Vol 16 (5) ◽  
pp. 512-521 ◽  
Author(s):  
Nidhi Rani ◽  
Randhir Singh
Keyword(s):  
Sulfonic Acid ◽  
Docking Study ◽  
Molecular Docking Study ◽  
One Pot ◽  
Design Synthesis ◽  
Toluene Sulfonic Acid ◽  
Antimicrobial Evaluation ◽  
Bacteria And Fungi ◽  
High Yields ◽  
Antimicrobial Potency

Background: A series of novel substituted 2-mercaptoimidazoles was synthesised efficiently and in high yields using one-pot synthesis from m-hydroxyacetophenones. Methods: The structures of the newly synthesized compounds were established, their molecular activity was investigated against some bacteria and fungi were further validated using molecular docking study. Results: Reaction of o-hydroxyphenacylbromide (2) with substituted aniline and KSCN, in the presence of catalyst p-toluene sulfonic acid afforded 4(a-r) in good yield. The structure of compounds (4a-r) was confirmed by IR, NMR and MS. Conclusion: The compounds exhibited excellent antimicrobial potency against the tested microorganism.

scholarly journals A Simple and Green Protocol for 2H-Indazolo[2,1-b]phthalazine-triones Using Grinding Method

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Xiao-chuan Jia ◽  
Jing Li ◽  
Yu Ding ◽  
Bin Zhang ◽  
Na Wang ◽  
...  
Keyword(s):  
Reaction Time ◽  
Sulfonic Acid ◽  
Catalytic Amount ◽  
Solvent Free ◽  
Short Reaction Time ◽  
Green Protocol ◽  
Simple Operation ◽  
Grinding Method ◽  
Toluene Sulfonic Acid ◽  
High Yields

A robust, facile, and solvent-free route for the three-component synthesis of 2H-indazolo[2,1-b]phthalazine-triones in the presence of a catalytic amount ofp-toluene sulfonic acid utilizing grinding has been developed. Short reaction time, simple operation, and high yields are the advantages of this protocol.

Synthesis of fatty 1,2,4-trioxanes by peracetalisation of β-hydroxy hydroperoxides

Synthesis ◽  
2021 ◽  
Author(s):  
Thomas De Dios Miguel ◽  
Dan Louvel ◽  
Killian Onida ◽  
Adeline Lavoignat ◽  
Stephane Picot ◽  
...  
Keyword(s):  
Sulfonic Acid ◽  
Heterogeneous Catalysts ◽  
Antimalarial Activity ◽  
Acid Catalyst ◽  
Methyl Tert Butyl Ether ◽  
Significant Activity ◽  
Butyl Ether ◽  
Aliphatic Aldehydes ◽  
Toluene Sulfonic Acid ◽  
Optimized Conditions

The peracetalisation of a β-hydroxy hydroperoxide derived from methyl oleate was studied using benzaldehyde as a model substrate to give the corresponding fatty 1,2,4-trioxane. The desired product was obtained as a mixture of regioisomers but only one diastereoisomer of each was formed. The nature of the acid catalyst was studied and both para-toluene sulfonic acid (PTSA) and Amberlyst A35 (A35) were found to be efficient homogeneous and heterogeneous catalysts, respectively. The nature of the solvent was also investigated and ethereal solvents such as 2-methyltetrahydrofuran (2-MeTHF), methyl tert-butyl ether (MTBE) and cyclopentyl methyl ether (CPME) gave the best NMR yield (85%) for the preparation of the fatty trioxane. The optimized conditions were applied to a range of aromatic and aliphatic aldehydes and the corresponding 1,2,4-trioxanes were isolated with 30-91% yields (21 examples). The antimalarial activity of 3 trioxanes was studied against Plasmodium falciparum, however, no significant activity was detected (IC50 > 1600 nM).

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