Home Chemistry Heterocyclic Building Blocks Pyridines 2-(Trifluoromethoxy)Pyridine
Nucleophilic substitution: The trifluoromethoxy group can be replaced by a nucleophile in substitution reactions. For example, reaction with strong nucleophiles such as amines can lead to the formation of substituted pyridines.
Electrophilic aromatic substitution: The electron-rich pyridine ring can undergo electrophilic aromatic substitution reactions. For instance, it can react with electrophiles such as acyl halides or alkyl halides to form substituted products.
Metalation reactions: The pyridine ring can be metalated at the 2-position, leading to the formation of organometallic compounds. These intermediates can further participate in various organic transformations.
Cross-coupling reactions: Trifluoromethoxypyridine can participate in cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig reactions, to form biaryl or heteroaryl compounds.
Oxidation and reduction reactions: The functional groups present in 2-(trifluoromethoxy)pyridine can undergo oxidation or reduction reactions under suitable conditions, leading to the formation of different products.
Formation of heterocyclic compounds: Due to its pyridine ring, 2-(trifluoromethoxy)pyridine can participate in various heterocyclic synthesis reactions, such as cyclization reactions with appropriate reagents.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
6-Chloro-3-iodo-2-(trifluoromethoxy)pyridine
click to sign in and save
(6-(Trifluoromethoxy)pyridin-3-yl)methanol
click to sign in and save
2-(Trifluoromethoxy)pyridine-3-carboxylic acid
click to sign in and save
(6-(Trifluoromethoxy)pyridin-3-yl)boronic acid
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :