Home Chemistry Heterocyclic Building Blocks Pyridines 1-(Pyridin-3-Yl)Ethan-1-One
Nucleophilic Addition Reactions: The carbonyl group of the ketone can undergo nucleophilic addition reactions. For example, it can react with Grignard reagents or organolithium compounds to form tertiary alcohols after protonation.
Aldol Condensation: 3-Acetylpyridine can undergo aldol condensation, similar to other ketones. Under basic conditions, it can react with itself or other carbonyl compounds to form β-hydroxy ketones, which may undergo further dehydration to form α,β-unsaturated ketones.
Friedel-Crafts Acylation: It can undergo Friedel-Crafts acylation reaction with acyl halides or acid anhydrides in the presence of a Lewis acid catalyst to form aryl ketones.
Oxidation: The ketone group can be oxidized to a carboxylic acid using strong oxidizing agents like potassium permanganate or chromic acid.
Reduction: The ketone group can be reduced to a secondary alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Halogenation: The aromatic ring can undergo electrophilic aromatic substitution reactions such as halogenation, where one or more hydrogen atoms on the ring are replaced by halogen atoms (e.g., bromination or chlorination).
Acylation: The nitrogen atom in the pyridine ring can be acylated using acyl chlorides or acid anhydrides in the presence of a Lewis acid catalyst to introduce acyl groups onto the nitrogen atom.
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1-(5-Bromo-6-(trifluoromethyl)pyridin-3-yl)ethanone
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1-(6-(Trifluoromethyl)pyridin-3-yl)ethanone
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1-(4-Chloropyridin-3-yl)ethanone hydrochloride
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1-(4-(Trifluoromethyl)pyridin-3-yl)ethanone
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1-(6-Amino-5-methylpyridin-3-yl)ethanone
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