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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222339생성일: 2026년 10월 24일

Hydrogen Peroxide → 3-Fluoro-2-(trifluoromethyl)phenol

https://huagongshe.com/ko/reaction/222339

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Trimethyl borateHCID 8470—
반응물Sodium HydroxideHCID 14798—
반응물2-Bromo-6-fluorobenzotrifluorideHCID 2773345—
반응물LithiumHCID 3028194—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Fluoro-2-(trifluoromethyl)phenolHCID 2497198240%

반응 단계

A solution of 3-fluoro-2-(trifluoromethyl)bromobenzene (1 g, 4.1 mmol) in tetrahydrofuran (25 mL) was added dropwise to nbutyl lithium (2.5M in hexanes, 3.2 mL, 8 mmol), at −78° C., and the mixture was stirred at this temperature for 30 minutes. Trimethyl borate (1.84 mL, 16.4 mmol) was added and the reaction mixture was stirred at −78° C. for a further 30 minutes and at room temperature for 18 hours. 2M sodium hydroxide solution (4 mL) and 35% hydrogen peroxide solution (2 mL) were then added and the mixture was heated under reflux for 3 hours. The reaction mixture was cooled to room temperature and diluted with diethyl ether (100 mL). The aqueous layer was separated and the organic solution was washed with 2M sodium hydroxide solution. The combined basic washings were acidified with 2M hydrochloric acid, extracted with diethyl ether (2×50 mL) and the organic solution was concentrated in vacuo to afford the title compound as a yellow oil in 40% yield, 300 mg. 1H NMR (400 MHz, CD3OD) δ: 6.64 (m, 1H), 6.75 (d, 1H), 7.36 (q, 1H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207198B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-4163f46eeefb46d8bc31f4ed23d3bbf9
출처 메모uspto-grants-2012_06