Chemistry Heterocyclic Building Blocks Pyridines 3-ethylpyridine
Ambeed provide 11 derivatives of 3-ethylpyridine.
These compounds have the same murcko framework: 3-ethylpyridineElectrophilic Substitution: Like other substituted pyridines, 3-ethylpyridine can undergo electrophilic substitution reactions at the 2-, 4-, and 6-positions on the pyridine ring. This includes reactions such as nitration, halogenation, and Friedel-Crafts acylation or alkylation.
Nucleophilic Substitution: If there are appropriate leaving groups present, nucleophilic substitution reactions can occur. For instance, substitution reactions at the 2-position can take place if a good leaving group is present at this position.
Oxidation: The alkyl group in 3-ethylpyridine can undergo oxidation reactions, especially under strong oxidizing conditions, leading to the formation of various oxidation products.
Reduction: Similarly, the nitrogen atom in the pyridine ring can be reduced under appropriate conditions, yielding different reduction products.
Alkylation/Acylation of the Nitrogen Atom: The nitrogen atom in the pyridine ring can undergo alkylation or acylation reactions under suitable conditions.
Condensation Reactions: 3-Ethylpyridine can participate in condensation reactions with appropriate reagents, leading to the formation of various condensed products.
Metal Complexation: The nitrogen atom of the pyridine ring can act as a ligand and form coordination complexes with transition metals.
Ring-opening Reactions: Under certain conditions, 3-ethylpyridine may undergo ring-opening reactions, leading to the formation of open-chain compounds.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
Deals click to sign in and save
5-Ethyl-2-(trifluoromethyl)pyridine