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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33507Generated: October 29, 2026

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

https://huagongshe.com/reaction/33507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl-6-(4-trifluoromethyl-phenyl)-pyridineHCID 69106617—
Reactant3-Methyl-4-(4-[1,2,3]triazol-1-yl-butyl)phenolHCID 69109666—
SolventDimethylformamideHCID 6228—
Product2-[3-Methyl-4-(4-[1,2,3]triazol-1-yl-butyl)-phenoxymethyl]-6-(4-trifluoromethyl-phenyl)-pyridineHCID 1606558284%

Reaction Conditions

Temperature0 °C

Reaction Steps

16 mg (0.39 mmol) of 95% sodium hydride were added at 0° C. to a solution of 86 mg (0.37 mmol) 3-methyl-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. 100 mg (0.37 mmol) 2-chloromethyl-6-(4-trifluoromethyl-phenyl)-pyridine were given to the reaction mixture and stirring continued at r.t overnight. After addition of 8 ml water the mixture was stirred for 1 h, the formed precipitate isolated by filtration, washed with water, methanol/water 1:1, and a small amount of ether. The residue was dried at 40° C. to give 145 mg (84%) of the title compound as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-0a1503599fa9477d8024684024b47c92
Source noteuspto-grants-2008_09