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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940722Generated: November 1, 2026

Dimethylformamide → 3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(2-chloro-4-trifluoromethylbenzyloxy)phenyl]-1-methyl-1H-1,2,4-triazole

https://huagongshe.com/reaction/1940722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-1-(chloromethyl)-4-(trifluoromethyl)benzeneHCID 21463657—
ReactantHCID 136048655HCID 136048655—
SolventWaterHCID 962—
Product3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(2-chloro-4-trifluoromethylbenzyloxy)phenyl]-1-methyl-1H-1,2,4-triazoleHCID 2146367672.8%

Reaction Steps

To 20 ml of N,N-dimethylformamide are added 3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-hydroxyphenyl)-1-methyl-1H-1,2,4-triazole (0.70 g) and potassium carbonate (0.31 g) and 2-chloro-4-trifluoromethylbenzyl chloride (0.50 g) is added thereto at room temperature with stirring, which is stirred at 120° C. for 5 hours. On completion of the reaction, the reaction solution is cooled to room temperature, poured into water and extracted with ethyl acetate. The organic layer is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography to give 0.80 g of desired compound (melting point: 156.0°-159.0° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700824
Source datasetuspto-grants-1997_12
ORD IDord-c598666fa7324a0bae76fe680e584763
Source noteuspto-grants-1997_12