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HRID 567873作成日:2026年10月26日

3,5-Dimethoxyphenol → 2-(3,5-Dimethoxyphenoxy)-6-fluorophenyl acetic acid

https://huagongshe.com/reaction/567873

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethoxyphenolHCID 10383—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-6-fluorophenylacetic acidHCID 123464—
触媒CopperHCID 23978—
触媒Copper iodideHCID 83717—
溶媒DimethylformamideHCID 6228—
生成物2-(3,5-Dimethoxyphenoxy)-6-fluorophenyl acetic acidHCID 5436934286.1%

反応条件

温度120 °C

反応手順

N,N-Dimethylformamide (20 ml) was added to 2-chloro-6-fluorophenyl acetic acid (3.77 g), 3,5-dimethoxyphenol (3.08 g), potassium carbonate (5.52 g), copper iodide (950 mg) and copper (250 mg), for stirring at 120° C. for 20 hours. The resulting solution was partitioned between ethyl acetate and dilute hydrochloric acid, and the organic phase was washed in water and in an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, to distill off the solvents under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3), to recover 2-(3,5-dimethoxyphenoxy)-6-fluorophenyl acetic acid (5.27 g; yield of 86%). By 2H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06180659B2
出典データセットuspto-grants-2001_01
ORD IDord-efbdaef15b4a47079767403f833f42af
出典メモuspto-grants-2001_01