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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 578804생성일: 2026년 10월 26일

Sodium Sulfite → 2,3-Difluoro-6-methoxyphenol

https://huagongshe.com/reaction/578804

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfiteHCID 24437—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물2,3-Difluoro-6-methoxybenzaldehydeHCID 2774112—
용매DichloromethaneHCID 6344—
생성물2,3-Difluoro-6-methoxyphenolHCID 326972870.8%

반응 단계

To a solution of 2,3-difluoro-6-methoxybenzaldehyde (2.58 g) in methylene chloride (45 mL) was added 3-chloroperbenzoic acid (5.97 g) under ice-cooling, and the mixture was heated for reflux overnight. The reaction mixture was cooled in ice. To the mixture was added 10% aqueous sodium sulfite solution, and the resulting mixture was stirred for 20 minutes. The organic layer was separated and washed with water twice, a saturated aqueous sodium hydrogen carbonate solution, water and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was dissolved in tetrahydrofuran (15 mL)-methanol (7.5 mL). To the solution was added sodium methoxide (28% methanol solution, 3.75 mL), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane−n-hexane/ethyl acetate=2/3) and column chromatography on aminopropylated silica gel (eluent: ethyl acetate/methanol=9/1−3/2) successively to give the title compound (1.7 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040693B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-58326b823453412f8fe29a84a6459a3a
출처 메모uspto-grants-2015_05