Home Chemistry Heterocyclic building blocks Pyridines 2,6-dimethylpyridin-4-ol
Acetylation: The hydroxyl group can be acetylated with acetic anhydride or acetyl chloride to form the corresponding acetate ester.
Esterification: Reaction with carboxylic acids in the presence of an acid catalyst can lead to the formation of esters.
Oxidation: The hydroxyl group can be oxidized to a carbonyl group using oxidizing agents such as chromic acid, Jones reagent, or potassium permanganate.
Alkylation/Acylation: The pyridine nitrogen can undergo alkylation or acylation reactions under appropriate conditions.
Ether Formation: The hydroxyl group can react with alkyl halides or alkyl sulfonates to form ethers.
Reduction: The carbonyl group can be reduced to a primary alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Nucleophilic Substitution: The nitrogen atom in the pyridine ring can undergo nucleophilic substitution reactions with appropriate electrophiles.
Amination: The pyridine ring can be further functionalized through amination reactions, introducing amino groups.
Condensation Reactions: The hydroxyl group can participate in condensation reactions, such as the formation of ethers or esters.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :