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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1625199생성일: 2026년 10월 24일

Cesium carbonate → 4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid

https://huagongshe.com/ko/reaction/1625199

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Chloro-4-fluorophenolHCID 74814—
반응물2-Bromo-4-tert-butylbenzoic acidHCID 236352—
용매TolueneHCID 1140—
생성물4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acidHCID 5768770872.2%

반응 조건

온도120 °C

반응 단계

In a pressure-vessel, a stirring mixture of 2-bromo-4-tert-butylbenzoic acid (1.00 g, 3.89 mmol) and 2-chloro-4-fluorophenol (860 mg, 620 μL, 5.87 mmol) in toluene (20 mL) was added Cs2CO3 (2.53 g, 7.78 mmol) followed by copper(I) triflate benzene complex (98 mg, 0.19 mmol). The sealed vessel was heated to 120° C. for 16 h. After cooling to room temperature, the reaction mixture was partitioned between 50 mL EtOAc and 50 mL H2O. The aqueous layer was acidified using 2.0 N HCl(aq) and re-extracted with EtOAc. The combined organic solution was dried over Na2SO4, filtered, and concentrated. The residue was purified via silica gel chromatography using 0-3% MeOH/CH2Cl2 to give the product, 4-tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid as a white solid (907 mg, 2.81 mmol) in 72% yield. LC/MS: m/z 323.2 (M+H) at 1.99 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08779197B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-729cbca1987243dba6b471d9c68653b3
출처 메모uspto-grants-2014_07