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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437492생성일: 2026년 10월 25일

Pinacol → 3-[2-Chloro-4-(trifluoromethyl)phenoxy]benzoic acid

https://huagongshe.com/reaction/437492

반응식

참여 물질

역할이름HCID투입량
반응물PinacolHCID 6425—
반응물3-Hydroxybenzoic AcidHCID 7420—
반응물3,4-DichlorobenzotrifluorideHCID 9481—
반응물Potassium CarbonateHCID 11430—
용매Dimethyl SulfoxideHCID 679—
생성물3-[2-Chloro-4-(trifluoromethyl)phenoxy]benzoic acidHCID 91685—

반응 단계

To a 300 ml, 3-necked flask equipped with a condenser, stirrer, drying tube and thermometer is charged dimethylsulfoxide (100 ml), anhydrous potassium carbonate (30 g. >0.20 mole), 3,4-dichlorobenzotrifluoride (21.5 g., 0.10 mole), pinacol (10 g.) and 3-hydroxybenzoic acid (13.8 g., 0.10 mole). The reaction temperature is then taken slowly to 140°-5° C. while stirring vigorously and maintained as such for 4 days. The reaction mixture is then cooled to room temperature and the inorganic solids removed by filtration prior to pouring the filtrate into water (1200 ml). The aqueous solution is then triturated with CCl4 (2 × 200 ml), decanted and then acidified to pH1 (conc. HCl) to give a tan colored solid, 25,6 g., mp 114°-17° C. This solid is further purified by dissolving in CCl4 (500 ml) and drying with anhydrous MgSO4. The CCl4 solution is reduced in vacuo to give 19.6 g. (62%) of a yellow solid, mp 116°-19° C. Recrystallization of the yellow solid from hexane gives a tan colored solid, 3-(2-chloro-4-trifluoromethylphenoxy)-benzoic acid, mp 122°-3° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04031131
출처 데이터셋uspto-grants-1977_06
ORD IDord-ade202437c154813abd7b04ebec10f85
출처 메모uspto-grants-1977_06