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HRID 2229111作成日:2026年10月27日

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/reaction/2229111

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-Tris(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 15869678—
反応物Potassium methoxideHCID 23664618—
溶媒MethanolHCID 887—
生成物2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridineHCID 2257263043.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06420315B1
出典データセットuspto-grants-2002_07
ORD IDord-133fc0aeaa324d1ca22bbe29e71cb6a1
出典メモuspto-grants-2002_07