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HRID 573106作成日:2026年10月25日

Methyl 2,4-Difluorobenzoate → Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/573106

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2,4-DifluorobenzoateHCID 2782897—
反応物Potassium tert-butoxideHCID 23665647—
反応物6-(Benzyloxy)pyridin-3-olHCID 42553041—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoateHCID 67228431—

反応条件

温度75 °C

反応手順

To 6-(benzyloxy)pyridin-3-ol (1.10 g) in 2-methyltetrahydrofuran (20 mL) was added potassium t-butoxide (5.47 mL, 1.0M in tetrahydrofuran). After stirring for 15 minutes, methyl 2,4-difluorobenzoate (1.035 g) in 2-methyltetrahydrofuran (2 mL) was added and the reaction heated to 75° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (150 mL), washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (SF40-80 g) eluting with a gradient of 5% to 20% 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-81af208bf7a94fb2b2b9fb56bc926999
出典メモuspto-grants-2015_05