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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567870생성일: 2026년 10월 26일

2,5-Difluorobenzaldehyde → 1-(2,5-Difluorophenyl)ethan-1-one

https://huagongshe.com/reaction/567870

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DifluorobenzaldehydeHCID 137663—
반응물Magnesium methylbromideHCID 86584079—
용매TetrahydrofuranHCID 8028—
생성물1-(2,5-Difluorophenyl)ethan-1-oneHCID 7479484%

반응 단계

A solution of 2,5-difluorobenzaldehyde (24.6 g) in tetrahydrofuran (100 ml) was added dropwise to an ice-cooled solution (207 ml) of 0.92N magnesium methylbromide in tetrahydrofuran. The resulting solution was stirred at room temperature for 1.5 hours, and the organic phase was washed in an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, to subsequently distill off the solvents under reduced pressure. To the residue were added anhydrous dichloromethane (500 ml), sodium acetate (14.2 g) and pyridinium chlorochromate (55.94 g), prior to stirring at room temperature for 10 hours. To the resulting mixture was added an aqueous saturated sodium hydrogen carbonate solution, prior to extraction in ethyl acetate three times. 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=85:15), to recover 2′,5′-difluoroacetophenone (22.73 g; yield of 84%). By 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06180659B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-9b5ae262e48143f788a22aa8f902efee
출처 메모uspto-grants-2001_01