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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33486Generated: October 26, 2026

Water → 2-Methyl-3-[4-(4-[1,2,3]triazol-1-yl-butyl)-phenoxymethyl]-6-(4-trifluoromethyl-phenyl)-pyridine

https://huagongshe.com/reaction/33486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-[1,2,3]Triazol-1-yl-butyl)phenolHCID 12109494—
Reactant3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridineHCID 21935751—
SolventDimethylformamideHCID 6228—
Product2-Methyl-3-[4-(4-[1,2,3]triazol-1-yl-butyl)-phenoxymethyl]-6-(4-trifluoromethyl-phenyl)-pyridineHCID 1606503282%

Reaction Conditions

Temperature0 °C

Reaction Steps

14 mg (0.55 mmol) of 95% sodium hydride were added to at 0° C. to a solution of 109 mg (0.50 mmol) 4-(4-[1,2,3]triazol-1-yl-butyl)-phenol in 4.0 ml N,N-dimethylformamide and stirred for 30 min. at 0° C. 143 mg (0.50 mmol) 3-chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine were given to the reaction mixture and stirring continued at room temperature (r.t.) overnight. After addition of 8 ml water the mixture was stirred for 1 h, the formed precipitate isolated by filtration, washed twice with water, and twice with heptane. The residue was dried at 40° C. in vacuum to give 191 mg (82%) of the title compound as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-2a2be10914eb456f900cb9bb034cab00
Source noteuspto-grants-2008_09