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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623696Generated: October 29, 2026

Potassium Carbonate → 4-[[2-(4-fluorophenyl)-5-methyl-2H-1,2,3-triazol-4-yl]oxy]-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/623696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-2-(trifluoromethyl)pyridineHCID 14761442—
Reactant2-(4-fluorophenyl)-2,3-dihydro-5-methyl-4H-1,2,3-triazol-4-oneHCID 90110837—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-[[2-(4-fluorophenyl)-5-methyl-2H-1,2,3-triazol-4-yl]oxy]-2-(trifluoromethyl)pyridineHCID 90110211—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-(4-fluorophenyl)-2,3-dihydro-5-methyl-4H-1,2,3-triazol-4-one (i.e. the product of Step C, 3.1 g, 16 mmol) in N,N-dimethylformamide (70 mL) was added anhydrous potassium carbonate (6.2 g, 45 mmol) under an atmosphere of nitrogen. 4-Chloro-2-trifluoromethyl-pyridine (2.9 g, 16 mmol) was added and the mixture was heated to 100° C. for 20 h. The reaction mixture was diluted with water, then extracted with diethyl ether. The organic layer was washed successively with water and saturated aqueous sodium chloride solution, dried (MgSO4), filtered, and concentrated under reduced pressure. The crude material was purified by chromatography on silica gel eluting with 0 to 20% ethyl acetate in hexanes to obtain the title compound (4.2 g) as a viscous light yellow oil that solidified upon standing to form an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302999B2
Source datasetuspto-grants-2016_04
ORD IDord-1b4c6226f4a74d8eb59ad27880081edf
Source noteuspto-grants-2016_04