Home Chemistry Heterocyclic Building Blocks Pyridines 5-Bromopyridin-3-Ol
Substitution Reactions: The bromine atom in 5-bromopyridin-3-ol can undergo substitution reactions, where it can be replaced by other nucleophiles. For example, it can undergo nucleophilic substitution with a strong nucleophile to replace the bromine atom with another functional group.
Acylation Reactions: The hydroxyl group in 5-bromopyridin-3-ol can undergo acylation reactions, where it can be acylated to form esters or amides.
Oxidation Reactions: The hydroxyl group can be oxidized to form aldehydes, ketones, or carboxylic acids under appropriate conditions.
Reduction Reactions: The bromine atom or the hydroxyl group can undergo reduction reactions to form different functional groups.
Metalation Reactions: The pyridine ring can undergo metalation reactions, where a metal atom or metal-containing reagent can replace one of the hydrogen atoms on the pyridine ring.
Condensation Reactions: 5-bromopyridin-3-ol can participate in condensation reactions, where it can react with other molecules to form new chemical bonds and generate products such as heterocyclic compounds.
Alkylation Reactions: The hydroxyl group or the pyridine ring can undergo alkylation reactions, where alkyl groups can be added to these functional groups.
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tert-Butyl (5-bromo-3-hydroxypyridin-2-yl)carbamate
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