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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33509Generated: October 29, 2026

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

https://huagongshe.com/reaction/33509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-(Chloromethyl)-6-(4-chlorophenyl)-2-methylpyridineHCID 19805446—
Reactant3-Methyl-4-(4-[1,2,3]triazol-1-yl-butyl)phenolHCID 69109666—
SolventDimethylformamideHCID 6228—
Product6-(4-Chloro-phenyl)-2-methyl-3-[3-Methyl-4-(4-[1,2,3]triazol-1-yl-butyl)-phenoxymethyl]-pyridineHCID 1606502691.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

33 mg (0.83 mmol) of 60% sodium hydride were added to at 0° C. to a solution of 172 mg (0.79 mmol) 3-methyl-4-(4-[1,2,3]triazol-1-yl-butyl)-phenol in 8.0 ml N,N-dimethylformamide and stirred for 30 min. at 0° C. 200 mg (0.79 mmol) 3-chloromethyl-6-(4-chloro-phenyl)-2-methyl-pyridine were given to the reaction mixture and stirring continued at room temperature (r.t.) overnight. After addition of 16 ml water the mixture was stirred for 1 h, the formed precipitate isolated by filtration, washed with water, water/methanol 1:1, ethyl acetate, and ether. 324 mg (91%) of the title compound were obtained as slightly beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-dcab2be3ec8b43c0a90b2053afc1e528
Source noteuspto-grants-2008_09