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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535675생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/535675

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroacetateHCID 7295—
반응물Potassium CarbonateHCID 11430—
반응물Potassium HydroxideHCID 14797—
반응물3-Bromo-5-fluoro-2-hydroxybenzaldehydeHCID 23148955—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물7-Bromo-5-fluorobenzofuran-2-carboxylic acidHCID 1798270163%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859534B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-5e519e47b4254bf38cafbd0db2f6a7ce
출처 메모uspto-grants-2014_10