Synthesis and determination of acidity strength of some new di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates
{"title":"Synthesis and determination of acidity strength of some new di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates","authors":"Faruk Kardaş, H. Yüksek, Zafer Ocak","doi":"10.51435/turkjac.1109562","DOIUrl":null,"url":null,"abstract":"In this study, seven novel di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates (4a-g) were synthesized from the rections of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) with di-(2-formyl-6-ethoxyphenyl) terephtalate (3). The compounds 4a-g were characterized using by IR, 1H-NMR, 13C-NMR and UV spectral data. In addition, 4 type compounds were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents such as isopropanol, tert-butanol, dimethyl ketone, N,N-dimethylformamide and the half-neutralization potential values and the corresponding pKa values were determined for all cases.","PeriodicalId":274781,"journal":{"name":"Turkish Journal of Analytical Chemistry","volume":"95 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Analytical Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51435/turkjac.1109562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, seven novel di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates (4a-g) were synthesized from the rections of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) with di-(2-formyl-6-ethoxyphenyl) terephtalate (3). The compounds 4a-g were characterized using by IR, 1H-NMR, 13C-NMR and UV spectral data. In addition, 4 type compounds were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents such as isopropanol, tert-butanol, dimethyl ketone, N,N-dimethylformamide and the half-neutralization potential values and the corresponding pKa values were determined for all cases.