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Sinteze substituiranih 2H-piran-2-onskih prekurzorjev za nadaljnje cikloadicijske reakcije z maleinanhidridom kot dienofilom
ID Kostanjšek, Žan (Author), ID Kranjc, Krištof (Mentor) More about this mentor... This link opens in a new window

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Abstract
V diplomskem delu sem raziskoval sinteze substituiranih 2H-piran-2-onov, ki predstavljajo pomembne prekurzorje za nadaljnje cikloadicijske reakcije z različnimi dienofili. Za sinteze 2H-piran-2-onov sem uporabljal najbolj enostavno in praktično »one pot« metodo. Na enem izmed 2H-piran-2-onov sem izpeljal tudi reakcijo odstranitve benzoilne zaščitne skupine; produkt opisane reakcije se lahko uporablja v nadaljnjih sintezah za uvedbo nove zaščitne skupine. Pripravljen 2H-piran-2-on sem reagiral z maleinanhidridom, pri čemer sem izoliral nastal biciklo[2.2.2]oktenski adukt. Vse končne produkte sem tudi analiziral in s tem potrdil njihovo molekulsko strukturo. Za analize sem uporabil NMR spektroskopijo, IR spektroskopijo, (MS) masno spektrometrijo in meritve tališč.

Language:Slovenian
Keywords:2H-piran-2-on, Diels–Alderjeva reakcija, maleinanhidrid, cikloadicijska reakcija
Work type:Bachelor thesis/paper
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2024
PID:20.500.12556/RUL-161070 This link opens in a new window
Publication date in RUL:06.09.2024
Views:30
Downloads:7
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Secondary language

Language:English
Title:Synthesis of substituted 2H-pyran-2-one precursors for further cycloaddition reactions with maleic anhydride as dienophile
Abstract:
In my diploma thesis I investigated the syntheses of substituted 2H-pyran-2-ones, which represent important precursors for further cycloaddition reactions with various dienophiles. For the syntheses of 2H-pyran-2-ones I used the most straightforward and practical "one-pot" method. On one of the 2H-pyran-2-ones I have also carried out a removal of the benzoyl protecting group; the product thus obtained can be used in further syntheses to introduce a new protecting group. The prepared 2H-pyran-2-one was reacted with maleic anhydride to isolate the resulting bicyclo[2.2.2]octene adduct. All the final products were also analysed to confirm their molecular structure. NMR spectroscopy, IR spectroscopy, (MS) mass spectrometry and melting point measurements were used for the analyses.

Keywords:2H-pyran-2-one, Diels–Alder reaction, maleic anhydride, cycloaddition reaction

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