Home Chemistry Organic Building Blocks Ketones Furan-2(5H)-One
Hydrolysis: Furan-2(5H)-one can undergo hydrolysis in the presence of an acid or base to yield γ-hydroxybutyric acid, a carboxylic acid.
Esterification: Furan-2(5H)-one can react with alcohols in the presence of an acid catalyst to form esters. This reaction is similar to Fischer esterification.
Reduction: The carbonyl group in furan-2(5H)-one can be reduced to produce γ-butyrolactone, which is the lactone form of the compound.
Ring-opening reactions: Furan-2(5H)-one can undergo ring-opening reactions with nucleophiles to form various products, including carboxylic acids, alcohols, or other compounds, depending on the nature of the nucleophile.
Aldol condensation: Furan-2(5H)-one can participate in aldol condensation reactions, particularly in the presence of strong bases, leading to the formation of β-ketoesters or β-diketones.
Michael addition: Furan-2(5H)-one can react in Michael addition reactions with nucleophiles, such as amines or thiols, to form adducts.
Diels-Alder reaction: Furan-2(5H)-one can participate as a dienophile in Diels-Alder reactions with dienes to form cycloadducts.
Oxidation: The compound can be oxidized to produce other functional groups or compounds, depending on the specific oxidizing agent used.
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5-Chloro-3-methyl-2,5-dihydrofuran-2-one
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