Home Chemistry Heterocyclic Building Blocks Pyrimidines 4-Phenoxypyrimidine
Substitution Reactions: The phenyl group can undergo substitution reactions. For example, it can undergo electrophilic aromatic substitution reactions like nitration, sulfonation, halogenation, and Friedel-Crafts acylation/alkylation.
Nucleophilic Substitution: The pyrimidine ring can undergo nucleophilic substitution reactions. For instance, the nitrogen atoms in the pyrimidine ring can react with electrophiles.
Alkylation/Acylation of the Nitrogen Atoms: The nitrogen atoms in the pyrimidine ring can be alkylated or acylated using appropriate reagents. This can lead to the formation of N-alkyl or N-acyl derivatives.
Reduction: The pyrimidine ring can be reduced using reducing agents to form dihydropyrimidines or further reduced to form tetrahydropyrimidines.
Oxidation: 4-Phenoxypyrimidine can be oxidized under certain conditions, leading to the formation of various oxidation products.
Hydrolysis: The compound can undergo hydrolysis reactions under acidic or basic conditions, leading to the cleavage of chemical bonds in the molecule.
Condensation Reactions: It can participate in condensation reactions with other compounds, such as aldehydes or ketones, to form new products.
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