An Efficient and Green Procedure for the Synthesis of Quinoxaline Derivatives using 3,5-Bis(trifluoromethyl)phenylammonium triflate (BFPAT) Organocatalyst

2020 ◽  
Vol 17 ◽  
Author(s):  
Samad Khaksar ◽  
Mandana Alipour ◽  
Zinatosadat Hossaini ◽  
Faramarz Rostami-Charati

Aims: Aims:The application of 3,5-Bis(trifluoromethyl) phenyl ammonium triflate(BFPAT) as a convenient and novel organocatalyst for the synthesis of quinoxalines. Background: Recently, ammonium triflate-based organocatalysts have been rapidly evolved, and most of them have been synthesized and utilized in several organic transformations. Objective: 1) introducing a new organocatalyst 2) introducing a practical method for the synthesis of quinoxalines 3) to overcome some problem in this method 4) using water as a green solvent. Method: A water solution (3 ml) of 1,2-dicarbonyl compounds (1 mmol) and aryl 1,2-diamines (1 mmol) was mixed with BFPAT (10 mol%), and the resulting mixture was stirred at rt for an appropriate time. Upon completion of the reaction, (monitored by TLC), the resultant was cooled with the ice bath, filtered and washed with ethanol and purified by recrystallization from hot ethanol to afford pure products. Result: A wide variety of quinoxaline derivatives was achieved by the reaction of various substituted o-phenylenediamines and 1,2-diketones in water. Conclusion: A simple and new ammonium triflate-based organocatalyst was shown to effectively promote the highly efficient synthesis of quinoxalines in water as a green reaction medium. Compared to prior studies, the substrate scope of the starting material was largely extended. In particular, the synthesis avoids the toxic metals in the products, which provides a green and practical method for organic synthesis. Other: In particular, the synthesis avoids the toxic metals in the products, which provides a green and practical method for organic synthesis.

Gels ◽  
2022 ◽  
Vol 8 (1) ◽  
pp. 54
Author(s):  
Laura Riva ◽  
Angelo Davide Lotito ◽  
Carlo Punta ◽  
Alessandro Sacchetti

Herein we report the synthesis of cellulose-based metal-loaded nano-sponges and their application as heterogeneous catalysts in organic synthesis. First, the combination in water solution of TEMPO-oxidized cellulose nanofibers (TOCNF) with branched polyethyleneimine (bPEI) and citric acid (CA), and the thermal treatment of the resulting hydrogel, leads to the synthesis of an eco-safe micro- and nano-porous cellulose nano-sponge (CNS). Subsequently, by exploiting the metal chelation characteristics of CNS, already extensively investigated in the field of environmental decontamination, this material is successfully loaded with Cu (II) or Zn (II) metal ions. Efficiency and homogeneity of metal-loading is confirmed by scanning electron microscopy (SEM) analysis with an energy dispersive X-ray spectroscopy (EDS) detector and by inductively coupled plasma-optical emission spectrometry (ICP-OES) analysis. The resulting materials perform superbly as heterogeneous catalysts for promoting the reaction between aromatic aldehydes and alcohols in the synthesis of aromatic acetals, which play a fundamental role as intermediates in organic synthesis. Optimized conditions allow one to obtain conversions higher than 90% and almost complete selectivity toward acetal products, minimizing, and in some cases eliminating, the formation of carboxylic acid by-products. ICP-OES analysis of the reaction medium allows one to exclude any possible metal-ion release, confirming that catalysis undergoes under heterogeneous conditions. The new metal-loaded CNS can be re-used and recycled five times without losing their catalytic activity.


2015 ◽  
Vol 5 (5) ◽  
pp. 2554-2574 ◽  
Author(s):  
Xiao-Yun Dong ◽  
Zi-Wei Gao ◽  
Ke-Fang Yang ◽  
Wei-Qiang Zhang ◽  
Li-Wen Xu

Silver nanoparticles catalysis has been of great interest in organic synthesis and has expanded rapidly in the past ten years because of nanosilver catalysts' unique reactivity and selectivity, stability, as well as recyclability in catalytic reactions.


RSC Advances ◽  
2016 ◽  
Vol 6 (59) ◽  
pp. 54449-54455 ◽  
Author(s):  
Bhavani Shankar Chinta ◽  
Beeraiah Baire

99% selectivity for cross coupling. Excellent yields (upto 94%). Low basic reaction medium, high functional group tolerance. Use of green solvent water.


2020 ◽  
Vol 24 ◽  
Author(s):  
Ghodsi Mohammadi Ziarani ◽  
Shima Roshankar ◽  
Fatemeh Mohajer ◽  
Alireza Badiei

Abstract:: Mesoporous silica nanomaterials provide an extraordinary advantage for making new and superior heterogeneous catalysts because of their surface silanol groups. The functionalized mesoporous SBA-15, such as acidic, basic, BrÖnsted, lewis acid, and chiral catalysts, are used for a wide range of organic synthesis. The importance of the chiral ligands, which were immobilized on the SBA-15, was mentioned in this review to achieve chiral products as valuable target molecules. Herein, their synthesis and application in different organic transformations are reviewed from 2016 till date 2020.


2019 ◽  
Vol 23 (11) ◽  
pp. 1214-1238 ◽  
Author(s):  
Navjeet Kaur ◽  
Pranshu Bhardwaj ◽  
Meenu Devi ◽  
Yamini Verma ◽  
Neha Ahlawat ◽  
...  

Due to special properties of ILs (Ionic Liquids) like their wide liquid range, good solvating ability, negligible vapour pressure, non-inflammability, environment friendly medium, high thermal stability, easy recycling and rate promoters etc. they are used in organic synthesis. The investigation for the replacement of organic solvents in organic synthesis is a growing area of interest due to increasing environmental issues. Therefore, ionic liquids have attracted the attention of chemists and act as a catalyst and reaction medium in organic reaction with high activity. There is no doubt that ionic liquids have become a major subject of study for modern chemistry. In comparison to traditional processes the use of ionic liquids resulted in improved, complimentary or alternative selectivities in organic synthesis. The present manuscript reported the synthesis of multiple nitrogen containing five-membered heterocyclic compounds using ionic liquids. This review covered interesting discoveries in the past few years.


2019 ◽  
Vol 23 (6) ◽  
pp. 643-678
Author(s):  
Lalthazuala Rokhum ◽  
Ghanashyam Bez

Recent years have witnessed a fast development of solid phase synthetic pathways, a variety of solid-supported reagent and its applications in diverse synthetic strategies and pharmaceutical applicability’s. Polymer-supported triphenylphosphine is getting a lot of applications owing to the speed and simplicity in the process. Furthermore, ease of recyclability and reuse of polymer-supported triphenylphosphine added its advantages. This review covers a wide range of useful organic transformations which are accomplished using cross-linked polystyrene-supported triphenylphosphine with the aim of giving renewed interest in the field of organic and medicinal-combinatorial chemistry.


2019 ◽  
Vol 16 (2) ◽  
pp. 258-275 ◽  
Author(s):  
Navjeet Kaur

Background:A wide variety of biological activities are exhibited by N, O and S containing heterocycles and recently, many reports appeared for the synthesis of these heterocycles. The synthesis of heterocycles with the help of metal and non-metal catalyst has become a highly rewarding and important method in organic synthesis. This review article concentrated on the synthesis of S-heterocylces in the presence of metal and non-metal catalyst. The synthesis of five-membered S-heterocycles is described here.Objective:There is a need for the development of rapid, efficient and versatile strategy for the synthesis of heterocyclic rings. Metal, non-metal and organocatalysis involving methods have gained prominence because traditional conditions have disadvantages such as long reaction times, harsh conditions and limited substrate scope.Conclusion:The metal-, non-metal-, and organocatalyst assisted organic synthesis is a highly dynamic research field. For ßthe chemoselective and efficient synthesis of heterocyclic molecules, this protocol has emerged as a powerful route. Various methodologies in the past few years have been pointed out to pursue more sustainable, efficient and environmentally benign procedures and products. Among these processes, the development of new protocols (catalysis), which avoided the use of toxic reagents, are the focus of intense research.


2020 ◽  
Vol 07 ◽  
Author(s):  
Avik K. Bagdi ◽  
Papiya Sikdar

Abstract:: Organic synthesis under environment friendly conditions has great impact in the sustainable development. In this context, visible light photocatalysis has emerged as a green model as this offers an energy-efficient pathway towards the organic transformation. Different transition-metal catalysts (Ir-, Ru-, Cu- etc) and organic dyes (eosin Y, rose bengal, methylene blue etc) are well-known photocatalysts in organic synthesis. Apart from the well-known organophotoredox catalysts, rhodamines (Rhodamine B and Rhodamine 6G) have been also employed as efficient photocatalysts for different organic transformations. In this review, we will focus on the photocatalysis by rhodamines in organic synthesis. Mechanistic pathway of the methodologies will also be discussed. We believe this review will stimulate the employment of rhodamines in the visible light photocatalysis for efficient organic transformations in the future.


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