Home Chemistry Heterocyclic Building Blocks Pyrimidines Pyrimidin-2-Ylmethanol
Nucleophilic Substitution: The hydroxyl group can act as a nucleophile and participate in nucleophilic substitution reactions. For example, it might react with an electrophile, such as an alkyl halide, in the presence of a base to form an ether linkage.
Oxidation: The hydroxymethyl group can be oxidized to a carboxyl group under certain conditions, typically involving oxidizing agents.
Esterification: The hydroxyl group can undergo esterification reactions with carboxylic acids or acid chlorides to form esters.
Nucleophilic Addition to Carbonyl Compounds: The pyrimidine ring can participate in nucleophilic addition reactions with carbonyl compounds (aldehydes or ketones) in the presence of a suitable catalyst, forming adducts.
Ring Closure Reactions: Depending on the conditions, the pyrimidine ring may undergo ring closure reactions, leading to the formation of various cyclic compounds.
Nucleophilic Aromatic Substitution: The nitrogen atoms in the pyrimidine ring can act as nucleophiles in certain conditions, participating in nucleophilic aromatic substitution reactions.
Reduction: The compound may undergo reduction reactions, for instance, converting the hydroxymethyl group to a methylene group.
Halogenation: The hydrogen atoms in the compound might be substituted with halogens under certain conditions, especially in the presence of halogenating agents.
Alkylation: The nitrogen atoms in the pyrimidine ring may undergo alkylation reactions with alkyl halides or similar electrophiles.
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(4-(Trifluoromethyl)pyrimidin-2-yl)methanol
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