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dc.contributor.advisorKasımoğulları, Rahmi
dc.contributor.authorDuran, Hamdiye
dc.date.accessioned2021-05-07T09:23:59Z
dc.date.available2021-05-07T09:23:59Z
dc.date.submitted2007
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/610995
dc.description.abstract4-ETOKS KARBON L-1-(3-N TROFEN L)-5-FEN L P RAZOL-3-KARBOKS L KAS T N SENTEZ VE REAKS YONLARIHamdiye DURANKimya Bölümü, Yüksek Lisans Tezi, 2006Tez Danışmanı: Yrd. Doç. Dr. Rahmi KASIMOĞULLARIÖZETBu çalışmada 4-Etoksi Karbonil-1-(3-Nitrofenil)-5-Fenil Pirazol-3-Karboksilik Asit'in(1) çeşitli nükleofillerle olan reaksiyonları araştırılmıştır. Bunun için ilk olarak etil-4,5-diokso-2-fenil-4,5-dihidrofuran 3-karboksilat bileşiğinin 3-nitrofenil hidrazonla reaksiyonundan yüksekbir verimle 1 bileşiği sentezlendi.Diğer yandan 1 bileşiğinin tiyonil klorür ile reaksiyonundan etil-3-(klorokarbonil)-1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat(2) bileşiği, bu bileşiğinde muhtelif alkol, amin veürelerle reaksiyonlarından, ester, amit ve üreid türevleri (3 ,4, 5, 6, 7, 8, 9, 10, 11, 12, 13)sentezlendi. Ayrıca 13 bileşiğinin soğukta DMF içerisinde SOCI2 ile reaksiyonu sonucu birkarbonitril türevi olan 14 bileşiğinin sentezi gerçekleştirildi. 1 bileşiğinin yüksek sıcaklıktadekarboksilasyonuyla 15 bileşiği elde edildi. Sentezlenen bütün bu bileşiklerin yapıları spektralmetotlarla aydınlatılmış olup, isimleri aşağıdaki şekilde sıralanabilir.4-(etoksikarbonil)-1-(3-nitrofenil)-5-fenil pirazol-3-karboksilik asit, Etil 3-(klorokarbonil)-1-(3-nitrofenil-5-fenil pirazol-4-karboksilat, 4-etil 3-metil 1-(3-nitrofenil)-5-fenil pirazol-3,4-dikarboksilat, dietil 1-(3-nitrofenil)-5-fenil pirazol-3,4-dikarboksilat, 4-etil 3-propil 1-(3-nitrofenil)-5-fenil pirazol-3,4-dikarboksilat, 4-etil 3-izopiropil 1-(3-nitrofenil)-5-fenil pirazol-3,4-dikarboksilat, 4-etil 3-fenil 1-(3-nitrofenil)-5-fenil pirazol-3,4-dikarboksilat,etil 3-(karbomoilkarbomoil)-1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat, etil 1-(3-nitrofenil)-5-fenil-3-(fenilkarbomoilkarbomoil) pirazol-4-karboksilat, etil 1-(3-nitrofenil)-3-(4-nitrofenilkarbomoil)-5-fenil pirazol-4-karboksilat, etil 3-(naftil-2-karbomoil)-1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat, etil 1-(3-nitrofenil)-5-fenil-3-(fenilkarbomoil)pirazol-4-karboksilat,etil 3-karbomoil-1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat, etil 3-siyano-1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat, etil 1-(3-nitrofenil)-5-fenil pirazol-4-karboksilat.Anahtar kelimeler: 4-etoksikarbonil-2-(3-nitrofenil)-5-fenil pirazol-3-karboksilik asit, pirazol,piridazin, nükleofilik katılma.
dc.description.abstractTHE SYNTHESIS AND REACTIONS OF 4-( ETHOXYCARBONYL)-1-( 3 -N TROPHENYL)-5-PHENYL PYRAZOLE-3-CARBOXYL C AC DHamdiye DURANChemistry Department, M.S. Thesis, 2006Thesis Supervisor: Yard. Doç. Rahmi KASIMOĞULLARISUMMARYIn this study, the reactions of 4- ( ethoxycarbonyl) -1- ( 3- nitrophenyl pyrazole -3-carboxylic acid (1) with various nükleofils. (1) compound, yield of was efficiently synthesiedfrom the reaction of ethyl 4,5-dioxo -2- fenil-4,5-dihidrofuran -3- carboksilat with 3-nitrofenil hydrazon. Besides, ethyl 3-(chlorocarbonyl) -1-(3-nitrophenyl) -5- phenyl pyrazole -4-carboxylate (2) compound was synthesized.The deriatives of amide, ester, amine and üreid were obtaired from the reaction of thiscompound with alchol, amine and üre (3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13) the 14 compound wasabtained from the reaction of 13 with DMF in SOCl2 solution at low temperature. 15 compoundwas synthesied from the decarboxcilation reaction of 1 at ambient temperature. The structuresof all these compounds, which were synthesized, were illuminated by means of spectralmethods. Their names can be enumerated like this.4- ethyl 3- methyl 1-(3-nitrophenl)-5-phenyl pyrazole-3,4-dicarboxylate, diethyl 1-(3-nitrophenyl)-5-phenyl pyrazole-3,4-dicarboxylate, 4-ethyl 3-propyl 1-(3-nitrophenyl) -5- phenylpyrazole -3,4-dicarboxylate, 4-ethyl 3-isopropyl 1-(3-nitrophenyl)-5-phenyl pyrazole -3,4-dicarboxylate, 4-ethyl 3-phenyl 1-(3-nitrophenyl)-5-phenyl pyrazole -3,4-dicarboxylate, ethyl 3-(carbamoylcarbamoly)-1-(3-nitrophenyl)-5-phenyl pyrazole-4-carboxylate, ethyl 1-(3-nitrophenyl)-5-phenyl-3-(phenylcarbamoylcarbamoyl) pyrazole-4-carboxlate, ethy 1-(3-nitrophenyl) -3-(4-nitrophenylcarbomoyl)-5-phenyl pyrazole-4-carboxylate, ethyl 3-(naphthalen-2-ylcarbamoyl)-1-(3-nitrophenyl)-5-phenyl pyrazole-4-carboxylate, ethyl 1-(3-nitrophenyl)-5-phenyl-3-(phenylcarbamoyl) pyrazole-4-carboxylate, ethyl 3-carbamoyl-1-(3-nitrophenyl)-5phenyl pyrazole-4-carboxylate, ethyl 3-cyano-1-(3-nitrophenyl)-5-phenyl pyrazole-4-carboxylate, ethyl 1-(3- nitrophenyl)-5-phenyl pyrazole -4- carboxylate.Key words : 4-(ethoxycarbonyl)-1-(3-nitrophenyl)-5-phenyl pyrazole-3-carboxylic acid,cylooddition, nucleophilic addition.en_US
dc.languageTurkish
dc.language.isotr
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAttribution 4.0 United Statestr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectKimyatr_TR
dc.subjectChemistryen_US
dc.title4-etoksi karbonil-1-(3-nitrofenil)-5-fenil pirazol-3-karboksilik asitin sentezi ve reaksiyonları
dc.title.alternativeThe synthesis and reactions of 4-(ethoxycarbonyl)-1-(3-nitrophenyl)-5-phenyl pyrazole-3-carboxylic acid
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentKimya Ana Bilim Dalı
dc.identifier.yokid201299
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityDUMLUPINAR ÜNİVERSİTESİ
dc.identifier.thesisid199427
dc.description.pages90
dc.publisher.disciplineDiğer


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