Home Chemistry Heterocyclic Building Blocks Pyridines 4-Methoxypyridine
Electrophilic aromatic substitution reactions: The methoxy group can direct electrophilic aromatic substitution reactions at the ortho, meta, or para positions of the pyridine ring.
Nucleophilic substitution reactions: The pyridine nitrogen atom can undergo nucleophilic substitution reactions, especially with alkylating agents or acylating agents.
Oxidation reactions: The electron-rich nature of the pyridine ring makes it susceptible to oxidation reactions under appropriate conditions.
Reduction reactions: Depending on the reaction conditions and reagents used, 4-methoxypyridine can undergo reduction reactions, potentially reducing the pyridine ring or the methoxy group.
Functional group transformations: The methoxy group can undergo various functional group transformations, such as ether cleavage or substitution reactions.
Metal-catalyzed reactions: 4-methoxypyridine can participate in metal-catalyzed reactions, including cross-coupling reactions or metal-mediated functionalization reactions.
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3-Fluoro-4-methoxypyridine-2-carboxylic acid
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Methyl 6-(chloromethyl)-4-methoxypicolinate
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2-(Chloromethyl)-4-methoxypyridine hydrochloride
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