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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33482Generated: October 26, 2026

Water → 5-[4-(4-[1,2,3]Triazol-1-yl-butyl)-phenoxymethyl]-[2-(4-trifluoromethyl-phenyl)]-pyridine

https://huagongshe.com/reaction/33482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-[1,2,3]Triazol-1-yl-butyl)phenolHCID 12109494—
Reactant5-Chloromethyl-2-(4-trifluoromethyl-phenyl)-pyridineHCID 21935775—
SolventDimethylformamideHCID 6228—
Product5-[4-(4-[1,2,3]Triazol-1-yl-butyl)-phenoxymethyl]-[2-(4-trifluoromethyl-phenyl)]-pyridineHCID 1606502971%

Reaction Conditions

Temperature0 °C

Reaction Steps

23 mg (0.90 mmol) of 95% sodium hydride were added at 0° C. to a solution of 163 mg (0.75 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. 204 mg (0.75 mmol) 5-chloromethyl-2-(4-trifluoromethyl-phenyl)-pyridine (WO 2005/049573) were given to the reaction mixture and stirring continued at r.t for 2 days. 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 purified by chromatography on silica (eluent: ethyl acetate) to give 240 mg 71% of the title compound as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-89a19ef0ed494e12aaf6cc388993ebae
Source noteuspto-grants-2008_09