Esvet, A.Adem, R.Cagla, A.Ertan, S.2025-05-102025-05-1020221021-998610.30492/IJCCE.2021.521495.44792-s2.0-85143363346https://doi.org/10.30492/IJCCE.2021.521495.4479https://hdl.handle.net/20.500.14720/2959In this study, 5-benzoyl-6-phenyl-4-(4-(trifluoromethoxy) phenyl)-1,2,3,4-tetrahydroxypyrimidine (1); 5-benzoyl-6-phenyl-4-(4-(trifluoromethoxy) phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (2) and 5-benzoyl-6-phenyl-4-(3,5-dimethoxy) phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (3) compounds were prepared via Biginelli condensation reaction using Metal-organic framework (MIL-101) as an active catalyst. It was established to be an active heterogeneous catalyst for a three-component Biginelli condensation reaction with good yields (75-80 %). Moreover, the catalyst could easily be recovered and recycled without any significant loss of its catalytic activity. Also the compounds 5-benzoyl-6-phenyl-3-acetyl-4-(4-hydroxyphenyl)-1,2,3,4-tetrahydrothioxypyrimidine (4) and 5-benzoyl-6-phenyl-3-acetyl-4-(4-trifluoromethoxy)phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (5) were obtained acetylation reaction. The structures were characterized on the basis of1H-NMR,13C-NMR, FT-IR, and elemental analysis. And also molecular characterizations of compound 4 were analyzed by X-ray crystal analysis. In addition, the corrosion inhibition activity of synthesized compounds was examined with theoretical calculation using DFT method at the level of B3LYP / 6-31G (d, p). © 2022, Iranian Institute of Research and Development in Chemical Industries. All rights reserved.eninfo:eu-repo/semantics/closedAccessBiginelliDftTetrahydropyrimidinesX-Ray Crystal AnalysisArticle415Q3Q316431656