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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338993생성일: 2026년 10월 23일

Dimethyl Sulfate → 2-Fluoro-3-methoxybenzoic acid

https://huagongshe.com/ko/reaction/338993

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Potassium CarbonateHCID 11430—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물2-Fluoro-3-hydroxybenzoic acidHCID 593637—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물2-Fluoro-3-methoxybenzoic acidHCID 339067994.1%

반응 단계

A suspension of 2-fluoro-3-hydroxybenzoic acid (12.0 g, 76.9 mmol) and potassium carbonate (23.4 g, 169 mmol) in acetone (154 mL) was stirred at ambient temperature for 1 hour. To the mixture was added dimethyl sulfate (21.8 mL, 231 mmol) and the mixture stirred at ambient temperature for 30 minutes then heated at reflux for 4 hours. The mixture was cooled to ambient temperature, filtered and concentrated under reduced pressure. The residue was dissolved in anhydrous THF (154 mL) and the solution cooled to 0° C. in an ice bath. To this solution was added LiOH—H2O (12.9 g, 307 mmol) followed by water (30 mL) and the resulting mixture stirred at ambient temperature for 3 hours. The mixture was concentrated under reduced pressure and the residue partitioned between water and ethyl acetate and the layers separated. The aqueous layer was acidified with 1N HCl solution and extracted with ethyl acetate. The combined organic extracts were washed with brine and dried (MgSO4), filtered and concentrated under reduced pressure to afford 2-fluoro-3-methoxybenzoic acid (12.31 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889704B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5310aa142b8646b999a7a345849ab2a2
출처 메모uspto-grants-2014_11