戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 573112作成日:2026年10月27日

Dimethylformamide → Methyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/573112

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl 2,4-DifluorobenzoateHCID 2782897—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-Chloro-3-fluoro-5-hydroxypyridineHCID 40424737—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoateHCID 86642876—

反応手順

To a solution of 6-chloro-5-fluoropyridin-3-ol (0.977 g) in 2-methyltetrahydrofuran (12 mL) was added potassium 2-methylpropan-2-olate (1.0M in tetrahydrofuran, 7.28 mL). After stirring for 15 minutes at room temperature, methyl 2,4-difluorobenzoate (1.710 g) was added as a solution in 2-methyltetrahydrofuran (2 mL) followed by N,N-dimethylformamide (2 mL) then the reaction was heated to 75° C. under a nitrogen atmosphere. After stirring overnight the reaction was cooled, diluted with ethyl acetate (100 mL) and washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (GraceResolv 40 g) eluting with a gradient of 2% to 15% ethyl acetate/hexanes gave the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029404B2
出典データセットuspto-grants-2015_05
ORD IDord-83abc5fa911a4bf9b6f6b3b079582642
出典メモuspto-grants-2015_05