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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1909554생성일: 2026년 10월 24일

Sodium Hydroxide → 2-(4-Fluoro-2-methylphenoxy)-2-methylpropanoic acid

https://huagongshe.com/ko/reaction/1909554

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoateHCID 67405334—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Fluoro-2-methylphenoxy)-2-methylpropanoic acidHCID 58566357—

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 번호US08598374B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-f85fb975686e43919b30ea0dd89f8d02
출처 메모uspto-grants-2013_12