Home Chemistry Heterocyclic Building Blocks Pyridines 3-Iodopyridine
Substitution Reactions: The iodine atom in 3-iodopyridine is susceptible to nucleophilic substitution reactions. It can be substituted by various nucleophiles such as amines, alkoxides, thiols, and organometallic reagents.
Metal-Catalyzed Cross-Coupling Reactions: 3-Iodopyridine can undergo cross-coupling reactions with various organometallic reagents in the presence of transition metal catalysts such as palladium, nickel, or copper catalysts. This reaction is widely used in synthetic organic chemistry for the formation of carbon-carbon bonds.
Electrophilic Aromatic Substitution Reactions: The pyridine ring in 3-iodopyridine can undergo electrophilic aromatic substitution reactions. For example, it can react with electrophiles such as acyl chloride, alkyl halides, or nitro groups under appropriate conditions.
Reductive Reactions: The iodine atom in 3-iodopyridine can undergo reductive elimination reactions under certain conditions, leading to the formation of other substituted pyridines or related compounds.
Functional Group Transformations: 3-Iodopyridine can also undergo various functional group transformations such as oxidation, reduction, and coupling reactions to introduce different functional groups onto the pyridine ring.
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4-Chloro-5-iodo-2-(trifluoromethyl)pyridine
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tert-Butyl (5-iodo-2-(trifluoromethyl)pyridin-4-yl)carbamate
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