scholarly journals HOMOGENEOUS VINYLATION OF 2-HYDROXY-2 PHENYLETHANICAL ACID

2018 ◽  
Vol 6 (11) ◽  
pp. 350-354
Author(s):  
Parmanov A.B. ◽  
Nurmanov S.E. ◽  
Tomash Maniecki ◽  
Ziyadullayev O.E. ◽  
Abdullayev J.U.

Homogeneous-catalytical vinylation of 2-hydroxy-2-phenylethanical acid was carried out. Influence of catalylists nature, temperature and duration reaction on yield of synthesized vinyl ester has been investigated. basis of natural raw materials. Based on vinyl esters of carboxylic acids, their polymers and copolymers with unsaturated compounds of the ethylene series, emulsifiers for emulsion paints have been obtained; compounds that improve the viscosity of lubricating oils and are used as crosslinking agents in the rubber industry. Synthesis of vinyl esters based on monobasic aliphatic acids has been studied by the example of acetic acid by many researchers. In this respect, the aromatic carboxylic acids remain unexplored. Goal: Synthesis of vinyl ester of mandelic acid by it’s reaction with acetylene in the presence of heterogeneous catalysts, investigation of the influence of the nature of catalysts and the reaction temperature on the yield of obtained product. Methodology: Catalytic systems based on AlCl3∙6H2O or zinc salt of mandelic acid with dimethylsulfoxide were prepared and heterogeneous catalytic vinylation of mandelic acid with acetylene was carried out and it’s vinyl ether was obtained. Scientific Novelty. The synthesis of vinyl ester of mandelic acid with it’s reactions with acetylene using the catalytic systems AlCl3∙6H2O-DMSO and (C6H5CH(OH)COO)2Zn-DMSO was carried out. Obtained Data: The vinyl ester of mandelic acid was synthesized by it’s vinylation in stationary heterogeneous conditions. The influence of the nature of the catalyst (AlCl3∙6H2O, (C6H5CH(OH)COO)2Zn), temperature and duration of the reaction on the yield of the product was investigated. Features: vinylation of hydroxy carboxylic acid was investigated; the catalytic systems AlCl3∙6H2O-DMSO and (C6H5CH(OH)COO)2Zn-DMSO are used; factors influencing the yield of vinyl ester of mindalic acid and optimal conditions of it’s synthesis were found.

1994 ◽  
Vol 368 ◽  
Author(s):  
David L. Cocke ◽  
Donald G. Naugle ◽  
Thomas R. Hess

ABSTRACTChemical reactions of metals and strongly interacting alloys such as Cu-Mn, Ni-Ti, Ni-Hf and Ni-Zr with oxygen and hydrogen play important roles in the preparation, activation, and regeneration of many important heterogeneous catalytic systems involving supported and unsupported metals and alloys. Recent advances in the understanding of metal and alloy oxidation is bringing new insight into the reactive design and activation of bi- and multi-metallic catalysts. By surface studies of oxidation, thermal annealing and reduction of selected alloys and their thin films and reaction layers and products we have been able to delineate the factors which are most important to the oxide formation processes and the oxide reduction processes. Reaction models developed from these results are permitting the design of new catalyst systems and providing long sought understanding to explain specific aspects of well established metallic catalysts.


2021 ◽  
Vol 9 ◽  
Author(s):  
Immandhi Sai Sonali Anantha ◽  
Nagaraju Kerru ◽  
Suresh Maddila ◽  
Sreekantha B. Jonnalagadda

The synthesis of dihydropyridines, valuable molecules with diverse therapeutic properties, using eco-friendly heterogeneous catalysts as a green alternative received significant consideration. By selecting appropriate precursors, these compounds can be readily modified to induce the desired properties in the target product. This review focused on synthesising diverse dihydropyridine derivatives in single-pot reactions using magnetic, silica, and zirconium-based heterogeneous catalytic systems. The monograph describes preparation techniques for various catalyst materials in detail. It covers facile and benign magnetic, silica, zirconium-based, and ionic liquid catalysts, exhibiting significant efficacy and consistently facilitating excellent yields in short reaction times and in a cost-effective way. Most of the designated protocols employ Hantzsch reactions involving substituted aldehydes, active methylene compounds, and ammonium acetate. These reactions presumably follow Knoevenagel condensation followed by Michael addition and intra-molecular cyclisation. The multicomponent one-pot protocols using green catalysts and solvents have admirably increased the product selectivity and yields while minimising the reaction time. These sustainable catalyst materials retain their viability for several cycles reducing the expenditure are eco-friendly.


2014 ◽  
Vol 69 (5) ◽  
Author(s):  
Rasidah Razali ◽  
Ho Chin Siong ◽  
Lai Sin Yuan ◽  
Sheela Chandren ◽  
Hadi Nur

The design and synthesis of particulate materials for new catalyst systems with novel properties remain a big challenge today. Here an attempt has been made to synthesize particulate materials for several heterogeneous catalytic systems, which contain examples from our recent research projects in this area. The particulate catalysts have been designed for single centre catalyst, phase-boundary catalyst, bifunctional catalyst, photocatalyst and chiral catalyst. In our current research, the synthesis of well-aligned titanium dioxide catalyst with very high length to the diameter ratio has also been demonstrated for the first time by sol-gel method under magnetic field with surfactant as the structure aligning agent. 


2011 ◽  
Vol 319-320 ◽  
pp. 107-115
Author(s):  
Mohammad Ebrahim Zeynali ◽  
S. Hakim

The diffusion processes taking place in heterogeneous catalytic systems have been discussed. Various diffusion mechanisms such as Knudsen diffusion, molecular diffusion, configurational diffusion and surface diffusion sensitivity in catalytic systems were investigated. The concentration gradients inside the catalyst pellet were obtained for various Thiele modulus. The Knudsen number was calculated and discussed for large and small pores. The transitional diffusion coefficient was determined for diethylbenzene. The experimental pore size distribution carves for an industrial and synthesized catalyst was obtained and the effect of pore size distribution on diffusion coefficient was discussed.


1988 ◽  
Vol 53 (8) ◽  
pp. 1636-1646 ◽  
Author(s):  
Viliam Múčka ◽  
Kamil Lang

Some physical and catalytic properties of the two-component copper(II)oxide-chromium(III)oxide catalyst with different content of both components were studied using the decomposition of the aqueous solution of hydrogen peroxide as a testing reaction. It has been found that along to both basic components, the system under study contains also the spinel structure CuCr2O4, chromate washable by water and hexavalent ions of chromium unwashable by water. The soluble chromate is catalytically active. During the first period of the reaction the equilibrium is being established in both homogeneous and heterogeneous catalytic systems. The catalytic activity as well as the specific surface area of the washed solid is a non-monotonous function of its composition. It seems highly probable that the extreme values of both these quantities are not connected with the detected admixtures in the catalytic system. The system under study is very insensitive with regard to the applied doses of gamma radiation. Its catalytic properties are changed rather significantly after the thermal treatment and particularly after the partial reduction to low degree by hydrogen. The observed changes of the catalytic activity of the system under study are very probably in connection with the changes of the valence state of the catalytically active components of the catalyst.


Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1680
Author(s):  
Marta A. Andrade ◽  
Luísa M. D. R. S. Martins

The selective oxidation of styrene under heterogeneous catalyzed conditions delivers environmentally friendly paths for the production of benzaldehyde, an important intermediate for the synthesis of several products. The present review explores heterogeneous catalysts for styrene oxidation using a variety of metal catalysts over the last decade. The use of several classes of supports is discussed, including metal–organic frameworks, zeolites, carbon materials and silicas, among others. The studied catalytic systems propose as most used oxidants tert-butyl hydroperoxide, and hydrogen peroxide and mild reaction conditions. The reaction mechanism proceeds through the generation of an intermediate reactive metal–oxygen species by catalyst-oxidant interactions. Overall, most of the studies highlight the synergetic effects among the metal and support for the activity and selectivity enhancement.


Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 500
Author(s):  
Vladimir Kapustin ◽  
Elena Chernysheva ◽  
Roman Khakimov

In recent years, there has been a trend in the global oil industry to improve the proportion of heavy high-sulfur crude oils in the total volume of extracted and processed resources, reserves of which are estimated at over 800 billion metric tons. Therefore, the main line of oil refining is processing of heavy crudes and residua to allow maximum use of the hydrocarbon potential and yield of high-margin products. Hydrogenation processes of heavy raw materials are most attractive in terms of product quality. This article analyzes tar hydrocracking processes that are either in operation or at the stage of full-scale testing. These include Veba Combi-Cracker (VCC), Uniflex, suspended-bed catalyst hydrocracking (ENI), and vacuum residue hydroconversion (TIPS RAS). These technologies use heterogeneous catalysts and are designed to obtain the largest possible amount of liquid products. This article discusses the features of each technology, highlights their advantages and disadvantages, shows the main approaches to process management, and speculates about the development of these technologies. Tar refining is a major process in heavy oil upgrading, and the development of efficient tar-processing methods will influence refinery configurations and management.


2021 ◽  
Vol 08 ◽  
Author(s):  
Vivek Srivastava

Background: Baylis-Hillman reaction suffers from the requirement of cheap starting materials, easy reaction protocol, possibility to create the chiral center in the reaction product has increased the synthetic efficacy of this reaction, and high catalyst loading, low reaction rate, and poor yield. Objective: The extensive use of various functional or non-functional ionic liquids (ILs) with organocatalyst increases the reaction rate of various organic transformations as a reaction medium and as a support to anchor the catalysts. Methods: In this manuscript, we have demonstrated the synthesis of quinuclidine-supported trimethylamine-based functionalized ionic liquid as a catalyst for the Baylis-Hillman reaction. Results: We obtained the Baylis-Hillman adducts in good, isolated yield, low catalyst loading, short reaction time, broad substrate scope, accessible product, and catalyst recycling. N-((E,3S,4R)-5-benzylidene-tetrahydro-4-hydroxy-6-oxo-2H-pyran-3-yl) palmitamide was also successfully synthesized using CATALYST-3 promoted Baylis-Hillman reaction. Conclusion: We successfully isolated the 25 types of Baylis-Hillman adducts using three different quinuclidine-supported ammonium-based ionic liquids such as Et3AmQ][BF4] (CATALYST-1), [Et3AmQ][PF6] (CATALYST-2), and [TMAAmEQ][NTf2](CATALYST-3) as new and efficient catalysts. Tedious and highly active N-((E,3S,4R)-5-benzylidene-tetrahydro-4-hydroxy-6-oxo-2H-pyran-3-yl) palmitamide derivative was also synthesized using CATALYST-3 followed by Baylis-Hillman reaction. Generally, all the responses demonstrated higher activity and yielded high competition with various previously reported homogenous and heterogeneous Catalytic systems. Easy catalyst and product recovery followed by six catalysts recycling were the added advantages of the prosed catalytic system.


2018 ◽  
Vol 2018 ◽  
pp. 1-18 ◽  
Author(s):  
Heng Zhang ◽  
Yulin Hu ◽  
Liying Qi ◽  
Jian He ◽  
Hu Li ◽  
...  

In recent decades, a great deal of attention has been paid to the exploration of alternative and sustainable resources to produce biofuels and valuable chemicals, with aims of reducing the reliance on depleting confined fossil resources and alleviating serious economic and environmental issues. In line with this, lignocellulosic biomass-derived lactic acid (LA, 2-hydroxypropanoic acid), to be identified as an important biomass-derived commodity chemical, has found wide applications in food, pharmaceuticals, and cosmetics. In spite of the current fermentation of saccharides to produce lactic acid, sustainability issues such as environmental impact and high cost derived from the relative separation and purification process will be growing with the increasing demands of necessary orders. Alternatively, chemocatalytic approaches to manufacture LA from biomass (i.e., inedible cellulose) have attracted extensive attention, which may give rise to higher productivity and lower costs related to product work-up. This work presents a review of the state-of-the-art for the production of LA using homogeneous, heterogeneous acid, and base catalysts, from sugars and real biomass like rice straw, respectively. Furthermore, the corresponding bio-based esters lactate which could serve as green solvents, produced from biomass with chemocatalysis, is also discussed. Advantages of heterogeneous catalytic reaction systems are emphasized. Guidance is suggested to improve the catalytic performance of heterogeneous catalysts for the production of LA.


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