First Sustainable Aziridination of Olefins Using Recyclable Copper-Immobilized Magnetic Nanoparticles

Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 563-566 ◽  
Author(s):  
Sylvestre Toumieux ◽  
Mohamad Khodadadi ◽  
Gwladys Pourceau ◽  
Matthieu Becuwe ◽  
Anne Wadouachi

The first copper-catalyzed aziridination of olefins using re­cyclable magnetic nanoparticles is described. Magnetic nanoparticles were modified with dopamine and used as a support to coordinate copper. The methodology was optimized with styrene as olefin and using [N-(p-toluenesulfonyl)imino]phenyliodinane (PhI=NTs) as nitrene source. A microwave irradiation decreased the reaction time by 4-fold compared to conventional heating method. The catalyst was recovered by simple magnetic extraction and could be reused successfully up to five times without significant loss of activity. The methodology was ­applied to a range of different olefins leading to moderate to excellent yields in the formation of the expected aziridine.

2018 ◽  
Vol 18 (1) ◽  
pp. 53
Author(s):  
Ratnaningsih Eko Sardjono ◽  
Iqbal Musthapa ◽  
Iis Rosliana ◽  
Fitri Khoerunnisa ◽  
Galuh Yuliani

A new versatile macromolecule cyclic C-3,7-dimethyl-7-hydroxycalix[4]resorcinarene (CDHHK4R) has been synthesized from a fragrance agent, 7-hydroxycitronellal, via microwave irradiation. The reaction utilized a domestic microwave oven at various irradiation time and power to yield an optimum condition. As a comparison, the conventional heating method was also employed for the synthesis of the same calix[4]resorcinarene. Compared to the conventional method, microwave-assisted reaction effectively reduced the reaction time, the amount of energy consumption and the waste production. It is found that the synthesis of CDHHK4R by microwave irradiation yielded 77.55% of product, higher than by conventional heating which was only 62.17%.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
L. Achutha ◽  
R. Parameshwar ◽  
B. Madhava Reddy ◽  
V. Harinadha Babu

Quinoxaline-incorporated Schiff bases(4a–j)were synthesized by the condensation of 2-[(3-methylquinoxalin-2-yl)oxy]acetohydrazide(3)with indole-3-carbaldehyde, furfuraldehyde, 5-(4-nitrophenyl)-2-furfuraldehyde, and substituted benzaldehydes under conventional and microwave irradiation methods. The microwave method was found to be remarkably successful with higher yields, less reaction time, and environmentally friendly compared to conventional heating method. The chemical structures of the synthesized compounds have been confirmed by analytical and spectral data. All the compounds have been evaluated for antitubercular and anti-inflammatory activities.


2001 ◽  
Vol 05 (04) ◽  
pp. 376-380 ◽  
Author(s):  
DOMINIC A. DAVIES ◽  
CHRISTINA SCHNIK ◽  
JACK SILVER ◽  
JOSE L. SOSA-SANCHEZ ◽  
PHILIP G. RIBY

The microwave heating synthesis of (phthalocyaninato)bis(chloro)silicon(IV) prepared from diiminoisoindolene and silicon tetrachloride in quinoline has been shown to be rapid (5 min reaction time compared to 30 min with thermal heating) and results in a high yield (91% compared to 71% using thermal heating). A modified microwave ashing furnace was used to heat the reaction mixture. The high yield has led to a reduction in the purification time to 1 h (compared to 4 h or more using conventional heating).


2017 ◽  
Vol 23 (3) ◽  
pp. 205-211
Author(s):  
Adriana Cristina N. de Melo ◽  
Ronaldo N. de Oliveira ◽  
João R. de Freitas Filho ◽  
Teresinha G. da Silva ◽  
Rajendra M. Srivastava

AbstractThe preparation of eight 2,3-unsaturated O-glycosides from D-glycals and alcohols, using montmorillonite K-10 as an acid catalyst, is described. The Ferrier rearrangement products were obtained in good yields using conventional heating and microwave irradiation but the reaction time was substantially reduced employing the latter procedure. The yields were slightly lower under microwave exposure. Five of the di-O-acetylated products were deacetylated to the glycosides in excellent yields. The acetylated products possess good anti-inflammatory property suggesting that the acetyl group plays an important role in reducing the inflammation. Among the compounds tested, glycosides containing thiophene as an aglycone present much better inflammation reducing characteristics than the analogues without this function.


2021 ◽  
Vol 37 (1) ◽  
pp. 01-24
Author(s):  
Ashutosh Pal ◽  
Krishnanka Shekhar Gayen

The present review collects an update of the reactions in the area of medicinal chemistry using microwave irradiation. This review come up with an overview of most salient reactions performed under microwave irradiation in the field of drug discovery. Moreover, chemists are preferring to use this reaction rapidly in the academic as well as pharmaceutical laboratory during their drug discovery and making library of compounds. This reaction is much greener using less amount and readily recyclable solvents or sometimes reaction process without solvents and product become much cleaner, often yields are better than the conventional heating. Microwave irradiation is now very robust instrument used in company in the field of drug discovery, due to reduce the reaction time from hour to minute or even second and efficiently creation of compound libraries through combinatorial methodology associated with drug discovery so that new therapeutic agents bring to the market quicker. Hopefully, we will observe in the future the use of microwave irradiation drugs for the patients and this technology will utilize increase in number extensively in the field of medicinal chemistry. As this is an exceedingly rapid evolution area, this review offers significant expertise to the interested readers.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Biswa Mohan Sahoo ◽  
B. V. V. Ravi Kumar ◽  
Jnyanaranjan Panda ◽  
S. C. Dinda

A rapid, improved, and ecofriendly synthesis of thiopyrimidines is carried out via one-pot multicomponent reaction of ethylcyanoacetate, substituted benzaldehydes, and thiourea in presence of ethanolic K2CO3 using microwave irradiation heating method. Excellent yields, shorter reaction time, and easy workup are the major advantageous features of this green protocol. So the application of multicomponent reactions involves the combination of multiple starting materials with different functional groups leading to the highly efficient and environmentally friendly construction of multifunctional drug molecules. The structures of the newly synthesized products were assigned on the basis of IR and 1HNMR spectral data.


2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Alex K. Koech ◽  
Anil Kumar ◽  
Zachary O. Siagi

The present technology of transesterification of vegetable oils to produce biodiesel, which is suited to replace petrodiesel, has economic challenges, and therefore, alternative sources are being explored. Microalgae, a renewable, third-generation biofuel resource, have the potential to become a viable feedstock due to their high oil content and environmentally friendly nature. The present study investigates the effect of microwave irradiation on the simultaneous extraction and transesterification of algae lipids to produce fatty acid methyl ester (FAME), in a batch reaction system using sulphuric acid catalyst. In situ transesterification combines the two steps of lipid extraction and transesterification into a single step. The microwave synthesis unit comprised of a 3-neck round bottom flask inside a 1300-Watt microwave oven, fitted with a quick-fit condenser and having an external stirrer. Response surface methodology (RSM) was used to analyse the influence of process variables, dry algae to methanol ratio 1 : 4 − 1 : 14   g / ml , algae biomass to catalyst ratio 1 : 0.0032 − 1 : 0.0368   wt % , and reaction time 1 − 11   min , at 500  rpm stirring rate for in situ reaction. FAME was analysed using gas chromatography (GC). The total lipid content of Arthrospira Spirulina platensis microalgae biomass was found to be 10.7 % by weight. The algae biomass also contained proteins at   51.83 % , moisture content at 7.8 % , and ash content 14.30 % by weight. RSM gave the optimum process conditions as dry algae biomass feed to methanol wt / vol ratio of 1 : 9, catalyst concentration of 2   wt % , and reaction time of   7   minutes   for a maximum FAME yield of 83.43   wt % . The major fatty acid composition of FAME was palmitic 43.83 % , linoleic   38.83 % , and linolenic 19.41 % . FAME properties obtained according to European Standards (EN 14214) and American Society for Testing and Materials (ASTM D 6751) standards were as follows: flash point 16 4 o C calorific value 32,911   kJ / kg , acid value 0.475 KOH / g , viscosity 4.45   m m 2 / s , and specific gravity   0.868 . The study showed that Arthrospira Spirulina platensis microalgae lipid FAME met the biodiesel standards (EN 14214 and ASTM D 6751) and has the potential to replace petrodiesel. Microwave irradiation increased the reaction rate resulting in a reduced reaction time of 7 minutes (as compared to 8 hours for conventional heating) and therefore was found to be a superior heating mode as compared to conventional heating.


2016 ◽  
Vol 19 (2) ◽  
pp. 64-70
Author(s):  
Phuong Hoang Tran ◽  
Vy Hieu Huynh ◽  
Hai Ngoc Tran ◽  
Thach Ngoc Le

Intramolecular Friedel–Crafts acylation of aryl acids is a “green” reaction and environmentally benign, generates some valuable intermediated compounds for pharmaceutical uses. In addition, metal triflates under microwave irradiation are efficient catalysts, solving many problems when using traditional Lewis acids. Gd(OTf)3/[BMI]BF4, a good catalyst for the intramolecular Friedel–Crafts acylation under mild condition with high yield, reduced the reaction time and pollution. Furthermore, Gd(OTf)3 in [BMI]BF4 was easily recovered and reused without significant loss of its activity


2019 ◽  
Vol 16 (6) ◽  
pp. 491-494
Author(s):  
Dinesh S. Gavhane ◽  
Aniket P. Sarkate ◽  
Kshipra S. Karnik ◽  
Shritesh D. Jagtap ◽  
Sajed H. Ansari ◽  
...  

A proficient, microwave mediated methodology using CuFe2O4 nanoparticle as the catalyst for S-arylation of substituted benzene boronic acids with thiophenol has been developed. In this method, the substituted thioethers were easily obtained through a C-S bond formation using microwave irradiation technique as well as conventional heating in the presence of CuFe2O4 nanoparticles with modest to excellent yields with the less reaction time. The ligand free microwave technique helped in the preparation of substituted thioethers in measurable amount within 10 mins. The same results were obtained with conventional heating in 12h. The reported method is economically efficient and an alternative to the initial existing method for the preparation of substituted thioethers.


2014 ◽  
Vol 471 (1-2) ◽  
pp. 37-44 ◽  
Author(s):  
Mahmoud Seifi ◽  
Maryam Hassanpour Moghadam ◽  
Farzin Hadizadeh ◽  
Safa Ali-Asgari ◽  
Jafar Aboli ◽  
...  

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