Home Chemistry Heterocyclic Building Blocks Pyridines (6-Methylpyridin-2-Yl)Methanol
Oxidation: The alcohol group in (6-methylpyridin-2-yl)methanol can undergo oxidation reactions to form aldehyde or carboxylic acid derivatives. Common oxidizing agents like chromic acid (H2CrO4), potassium permanganate (KMnO4), or Jones reagent (CrO3 in sulfuric acid) can be used for this purpose.
Esterification: (6-methylpyridin-2-yl)methanol can undergo esterification reactions with carboxylic acids and acid chlorides to form esters. This reaction typically requires a catalyst such as sulfuric acid or hydrochloric acid.
Nucleophilic substitution: The hydroxyl group in (6-methylpyridin-2-yl)methanol can undergo nucleophilic substitution reactions with various electrophiles, such as alkyl halides or acyl chlorides, to form substituted derivatives.
Alkylation or Acylation: The nitrogen atom in the pyridine ring can undergo alkylation or acylation reactions with alkyl halides or acyl halides, respectively, under appropriate conditions.
Reduction: The pyridine ring in (6-methylpyridin-2-yl)methanol can be reduced under certain conditions, for example, using hydrogen gas over a metal catalyst (e.g., palladium on carbon) to form piperidines.
Condensation reactions: (6-methylpyridin-2-yl)methanol may undergo condensation reactions with carbonyl compounds or other suitable reactants to form heterocyclic compounds.
Grignard reaction: (6-methylpyridin-2-yl)methanol can react with alkyl or aryl halides in the presence of magnesium metal to form Grignard reagents, which are versatile synthetic intermediates.
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(4-Chloro-6-methylpyridin-2-yl)methanol
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