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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876396생성일: 2026년 10월 25일

Dimethyl Sulfoxide → Ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate

https://huagongshe.com/reaction/1876396

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Potassium CarbonateHCID 11430—
반응물Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
반응물4-Fluoro-2-methylphenolHCID 136295—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoateHCID 67405334—

반응 단계

A solution of 4-fluoro-2-methylphenol (10 g, 79.28 mmol), ethyl 2-bromoisobutyrate (23.2 mL, 158.6 mmol), potassium carbonate (21.9 g, 158.6 mmol), and DMSO (80 mL) was stirred at room temperature for 72 hours. Water and ethyl acetate were added and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 mL) and the combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%) to afford ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate. To a solution of ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate (13.3 g, 55.44 mmol) in tetrahydrofuran (40 mL) and methanol (10 mL) was added NaOH (6.66 g, 166.32 mmol) in water (14 mL) and stirred overnight. The volatiles were removed in vacuo and acidified with concentrated HCl. The milky white solution was extracted with ethyl acetate, dried over sodium sulfate, filtered and concentrated in vacuo to give 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoic acid (658) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309600B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-6d6bb607b02143e09086c6f024ef9b8e
출처 메모uspto-grants-2012_11