Chemistry Heterocyclic Building Blocks Pyridines 2-chloro-4-ethoxypyridine
Substitution Reactions: The chlorine atom in 2-chloro-4-ethoxypyridine can undergo substitution reactions with various nucleophiles to replace the chlorine atom with another group. For instance, it can undergo nucleophilic substitution reactions with amines, thiols, or other nucleophiles to form substituted pyridine derivatives.
Ether Formation: The ethoxy group in 2-chloro-4-ethoxypyridine can participate in ether formation reactions, especially in the presence of strong bases or acid catalysts. This can lead to the formation of cyclic ethers or acyclic ethers.
Metalation Reactions: The pyridine ring in 2-chloro-4-ethoxypyridine can undergo metalation reactions with strong bases or metal reagents, leading to the formation of metal complexes.
Redox Reactions: 2-chloro-4-ethoxypyridine can undergo various redox reactions depending on the reaction conditions and the presence of other reagents. For instance, it can be oxidized to form pyridine N-oxide derivatives or reduced to form dihydropyridine derivatives.
Condensation Reactions: The ethoxy group in 2-chloro-4-ethoxypyridine can participate in condensation reactions, such as acylation or alkylation reactions, leading to the formation of more complex molecules.
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(6-Chloro-4-ethoxypyridin-3-yl)methanamine hydrochloride