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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366299Generated: October 23, 2026

2,4,6-Tris(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridine → 2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridine

https://huagongshe.com/en/reaction/366299

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Tris(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 15869678—
ReactantPotassium methoxideHCID 23664618—
SolventMethanolHCID 887—
Product2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridineHCID 2257263043.4%

Reaction Steps

A 3 ml aliquot of a 25 % solution of potassium methylate (10 mmol) in dry methanol is added to a solution of 5.7 g (10 mmol) 2,4,6-tris-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridine in 20 ml anhydrous methanol. After 2 hours at ambient temperature, the reaction mixture is heated to reflux. The solvent is removed under reduced pressure and ethyl acetate is added to the residue. The mixture is washed with a 2 N sodium hydroxide solution. After drying and filtration of the organic layer, the solvents are removed and the residue is washed with diisopropyl ether and pentane. Colorless crystals (1.9 g, 43 % yield) of melting point 107° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130188
Source datasetuspto-grants-2000_10
ORD IDord-6759362e203b434a933ffc01546fab73
Source noteuspto-grants-2000_10