Home Chemistry Heterocyclic Building Blocks Pyridines 2-Chloropyridin-3-Ol
Substitution Reactions: The chlorine atom (Cl) in the compound can undergo substitution reactions with various nucleophiles, such as amines or thiols, to replace the chlorine atom with a different functional group.
Oxidation: The hydroxyl group (OH) can undergo oxidation reactions under appropriate conditions to form either a ketone or a carboxylic acid derivative, depending on the reaction conditions and the oxidizing agent used.
Esterification: The hydroxyl group can react with carboxylic acids or acid chlorides in the presence of an acid catalyst to form esters.
Nucleophilic Addition: The pyridine ring can undergo nucleophilic addition reactions with strong nucleophiles at the C-3 position, leading to the formation of substituted pyridines.
Dehydration: Under certain conditions, the compound can undergo dehydration reactions, leading to the formation of unsaturated compounds.
Reduction: The compound can undergo reduction reactions, where the chlorine atom or the hydroxyl group is reduced to a different functional group.
Acetylation: The compound can undergo acetylation reactions, where the hydroxyl group is acetylated to form an acetate ester.
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2-Chloro-5-(trifluoromethyl)pyridin-3-ol
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