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HRID 1583703作成日:2026年10月27日

Water → 4-trifluoromethylphenyl N-(6-methoxy-2-pyridyl)-N-methylcarbamate

https://huagongshe.com/reaction/1583703

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物6-methoxy-N-methylpyridin-2-amineHCID 7019168—
反応物4-(Trifluoromethyl)phenyl carbonochloridateHCID 15917597—
溶媒AcetoneHCID 180—
生成物4-trifluoromethylphenyl N-(6-methoxy-2-pyridyl)-N-methylcarbamateHCID 1338757762%

反応手順

To the mixture of 1.38 g of 2-methoxy-6-methylaminopyridine and 1.38 g of anhydrous potassium carbonate in 20 ml of acetone was added dropwise the solution of 2.25 g of 4-trifluoromethylphenyl chloroformate in 20 ml of acetone under stirring at room temperature. The mixture was stirred for 30 minutes and then was refluxed for 2 hours. After the reaction mixture was cooled to room temperature, it was poured into water and the product was extracted with benzene. The benzene solution, successively washed with water and brine, was dried over anhydrous magnesium sulfate. The residue obtained by the removal of benzene under reduced pressure was chromatographed through silica gel column using benzene as an eluent to give 2.02 g of pure 4-trifluoromethylphenyl N-(6-methoxy-2-pyridyl)-N-methylcarbamate as solid in the yield of 62%. A part of the solid was recrystallized from hexane and crystalls having melting point of 85° to 86° C. were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04554012
出典データセットuspto-grants-1985_11
ORD IDord-baa0b19a408d4b28a849a04cd0e9275f
出典メモuspto-grants-1985_11