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HRID 578804作成日:2026年10月27日

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

https://huagongshe.com/reaction/578804

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium SulfiteHCID 24437—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物2,3-Difluoro-6-methoxybenzaldehydeHCID 2774112—
溶媒DichloromethaneHCID 6344—
生成物2,3-Difluoro-6-methoxyphenolHCID 326972870.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040693B2
出典データセットuspto-grants-2015_05
ORD IDord-58326b823453412f8fe29a84a6459a3a
出典メモuspto-grants-2015_05