Green Methodology Development for the Surfactant Assisted Williamson Synthesis of 4-Benzyloxy Benzoic Acid (Ether) in Aqueous Media

2020 ◽  
Vol 57 (2) ◽  
pp. 115-121 ◽  
Author(s):  
Sangita Mandal ◽  
Satyajit Biswas ◽  
Monohar Hossain Mondal ◽  
Bidyut Saha
2020 ◽  
Vol 22 (9) ◽  
pp. 5046-5056 ◽  
Author(s):  
Natalia V. Karimova ◽  
Man Luo ◽  
Vicki H. Grassian ◽  
R. Benny Gerber

The microscopic interpretation of the electronic structure and absorption spectra of BA in aqueous media through calculations restricted to small cluster models.


2000 ◽  
Vol 35-36 ◽  
pp. 597-607 ◽  
Author(s):  
S. Valange ◽  
J.-L. Guth ◽  
F. Kolenda ◽  
S. Lacombe ◽  
Z. Gabelica

Langmuir ◽  
2012 ◽  
Vol 28 (25) ◽  
pp. 9906-9906 ◽  
Author(s):  
Moumita Chakraborty ◽  
Fang-Wei Hsiao ◽  
Bappaditya Naskar ◽  
Chien-Hsiang Chang ◽  
Amiya Kumar Panda

RSC Advances ◽  
2016 ◽  
Vol 6 (81) ◽  
pp. 77870-77886 ◽  
Author(s):  
G. L. Perlovich

The dissolution processes in aqueous media of poorly soluble drugs belonging to the classes of spiro and benzoic acid derivatives, sulfonamides, fenamates, and thiadiazoles were analyzed based on the data recently published by the author.


2009 ◽  
Vol 6 (4) ◽  
pp. 985-992 ◽  
Author(s):  
Mohammad Saeid Hosseini ◽  
Sara Madarshahian

On the basis of affinity of Fe(III) ions toward functional groups of 2,6-dihydroxy benzoic acid (2,6-DHB), a charge transfer complex (CT) is formed between Fe(III) ion and 2,6-DHB in acidic media. The stoichiometry and stability constant of the complex was determined using both mole ratio and Job’s methods. The stability constant of 1:1 complex formed in acidic media is 2.55±0.14×105(mole ratio) or 2.70±0.12×105(Job), in which the quantities are in agreement with together. This method was used for spectrophotometric determination of Fe(III) in aqueous media. The dynamic range and detection limit (DL) were 1.2×10-5to 3.6×10-4M and 1.5×10-6M, respectively. The relative standard deviation (RSD) was found to be 0.76% in the replicate treatments (n=7) with 1.6×10-4M Fe(III). The practical applicability of the method was confirmed using a synthetic certificated reference material (CRM) and spiked natural water samples.


2020 ◽  
Vol 17 (34) ◽  
pp. 62-66
Author(s):  
Claudemir BATALINI ◽  
Wagner Ferraresi DE GIOVANI

Various organic functions can undergo oxidation reactions, and the chemical industry increasingly seeks to develop processes based on the Green Chemistry approach in the search for more sustainable practices. Electrochemical electron transfer processes using metal complexes thus appear as an important alternative in these oxidative processes since they exploit numerous reactions in aqueous media and use catalytic amounts of the complex. The purpose of this work was to test the electrocatalytic ability of a new ruthenium (II) diarsenic aqua complex, [Ru(L)(totpy)(OH2)](ClO4)2 (L=Ph2AsCH2CH2AsPh2); (totpy=4´-(4-tolyl)-2,2´:6´,2´´-terpyridine), in electrooxidation experiments of organic substances with different functions. The experiments were conducted at a constant potential of +1.00 V (vs ECS) in a solution of 7:3 phosphate buffer: t-butanol, pH 8.1, with a ratio of 1.00 mmol.L-1 of the aqua complex [Ru(L)(totpy)(OH2)](ClO4)2 to 50.00 mmol.L-1 of each organic substrate. The oxidized organic starting materials and the respective products obtained therefrom were benzyl alcohol (benzaldehyde), benzaldehyde (benzoic acid), benzyl butyl ether (benzaldehyde and benzoic acid) and 1-phenylethanol (acetophenone). Selective reactions with good yields for the products were observed. The electrochemical process used here revealed some benefits over other classic oxidative methods, such as biological advantages and inorganic oxidants, emphasizing the speed, the possibility of using aqueous media in the reactions, selectivity in the formation of products, and the possibility of using small amounts of catalyst.


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