戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 535675作成日:2026年10月26日

Methyl chloroacetate → 7-Bromo-5-fluorobenzofuran-2-carboxylic acid

https://huagongshe.com/reaction/535675

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroacetateHCID 7295—
反応物Potassium CarbonateHCID 11430—
反応物Potassium HydroxideHCID 14797—
反応物3-Bromo-5-fluoro-2-hydroxybenzaldehydeHCID 23148955—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物7-Bromo-5-fluorobenzofuran-2-carboxylic acidHCID 1798270163%

反応条件

温度130 °C

反応手順

Methyl chloroacetate (7.6 mL, 86.8 mmol) was added to a mixture of 3-bromo-5-fluoro-2-hydroxy-benzaldehyde (9.5 g, 43.4 mmol), tetra-N-butyl-ammonium iodide (1.6 g, 4.34 mmol) and anhydrous potassium carbonate (24 g, 174 mmol). The reaction mixture was heated at 130° C. for 4 h, cooled to 0° C., diluted with tetrahydrofuran (100 mL) and then potassium hydroxide (17 g, 303 mmol) in water (100 mL). The mixture was stirred at rt for 18 h and then, concentrated under reduced pressure. The residue was acidified with HCl and extracted with ethyl acetate. The combined organic extracts were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude compound was purified by flash chromatography (SiO2; toluene/EtOAc, 40/1) to give 7.0 g (63%) of the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859534B2
出典データセットuspto-grants-2014_10
ORD IDord-5e519e47b4254bf38cafbd0db2f6a7ce
出典メモuspto-grants-2014_10