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undergraduate thesis
Oksidacije 1-benzotiofena (tianaftena)
2012. urn:nbn:hr:182:705552
Glavaš, Mladena
Josip Juraj Strossmayer University of Osijek
Department of Chemistry

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Glavaš, M. (2012). Oksidacije 1-benzotiofena (tianaftena) (Undergraduate thesis). Osijek: Josip Juraj Strossmayer University of Osijek, Department of Chemistry. Retrieved from https://urn.nsk.hr/urn:nbn:hr:182:705552

Glavaš, Mladena. "Oksidacije 1-benzotiofena (tianaftena)." Undergraduate thesis, Josip Juraj Strossmayer University of Osijek, Department of Chemistry, 2012. https://urn.nsk.hr/urn:nbn:hr:182:705552

Glavaš, Mladena. "Oksidacije 1-benzotiofena (tianaftena)." Undergraduate thesis, Josip Juraj Strossmayer University of Osijek, Department of Chemistry, 2012. https://urn.nsk.hr/urn:nbn:hr:182:705552

Glavaš, M. (2012). 'Oksidacije 1-benzotiofena (tianaftena)', Undergraduate thesis, Josip Juraj Strossmayer University of Osijek, Department of Chemistry, accessed 17 November 2024, https://urn.nsk.hr/urn:nbn:hr:182:705552

Glavaš M. Oksidacije 1-benzotiofena (tianaftena) [Undergraduate thesis]. Osijek: Josip Juraj Strossmayer University of Osijek, Department of Chemistry; 2012 [cited 2024 November 17] Available at: https://urn.nsk.hr/urn:nbn:hr:182:705552

M. Glavaš, "Oksidacije 1-benzotiofena (tianaftena)", Undergraduate thesis, Josip Juraj Strossmayer University of Osijek, Department of Chemistry, Osijek, 2012. Available at: https://urn.nsk.hr/urn:nbn:hr:182:705552

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Metadata
TitleOksidacije 1-benzotiofena (tianaftena)
AuthorMladena Glavaš
MentorNela Malatesti (mentor)
GranterJosip Juraj Strossmayer University of Osijek
Department of Chemistry
Osijek
Defense date and country2012, Croatia
Scientific / art field,
discipline and subdiscipline		NATURAL SCIENCES
Chemistry
Abstract
Aromatski heterociklički spoj 1-benzotiofen, oksidacijom se prevodi iz sulfida u odgovarajući sulfon, 1 -benzotiofen-1,1-dioksid. U ovom radu 1 -benzotiofen je oksidiran u 1-benzotiofen-1,1-dioksid korištenjem vodene otopine vodikova peroksida i ledene octene kiseline kao otapala, uz refluksiranje i to u vrlo dobrom iskorištenju od 71 %. Oksidacija 1- benzotiofena je provedena i uz oksidirajući reagens H2O2-P2O5 i acetonitril kao otapalo, sa ili bez refluksiranja. Ovisno o metodi, iskorištenja su bila 3-48%. Korištenje H2O2-P2O5 reagensa je ekološki prihvatljivo i pokazalo se kao dosta dobro oksidacijsko sredstvo, koje se može primjeniti i za druge heterocikličke spojeve koji sadrže sumpor, a u slučaju 1 - benzotiofena osobito onda kada sadrži elektron-akceptorske skupine (EWG).
Abstract (english)
The aromatic heterocyclic compound 1-benzothiophene can be oxidized from its sulfide functional group into a sulfone, 1-benzothiophene-1,1-dioxide. In this work 1- benzothiophene is oxidized into 1 -benzothiophene-1,1-dioxide by heating an aqueous solution of hydrogen peroxide and glacial acetic acid as a solvent at reflux, with a very good yield of 71 %. Oxidation of 1-benzothiophene was carried out with H2O2-P2O5 reagent and acetonitrile as solvent, with and without reflux. Depending on the method, yields were ranging from 3-48%. The use of H2O2-P2O5 reagent is environmentally acceptable and it has been demonstrated to be a good oxidation agent which can be applied for other heterocyclic compound that contain sulfur, especially for 1-benzothiophenes that contain electron-withdrawing groups (EWG).
Keywords
Keywords (english)
Languagecroatian
URN:NBNurn:nbn:hr:182:705552
Study programmeTitle: Chemistry
Study programme type: university
Study level: undergraduate
Academic / professional title: sveučilišni/a prvostupnik/prvostupnica (baccalaureus/baccalaurea) kemije (sveučilišni/a prvostupnik/prvostupnica (baccalaureus/baccalaurea) kemije)
Type of resourceText
File originBorn digital
Access conditionsOpen access
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Created on2016-07-12 08:34:05