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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1025983생성일: 2026년 10월 25일

Hydrochloric Acid → 5-(3-Chloro-4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

https://huagongshe.com/reaction/1025983

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium CarbonateHCID 10340—
반응물3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 2734660—
반응물5-Bromo-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acidHCID 58192592—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물5-(3-Chloro-4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acidHCID 6667884263%

반응 조건

온도90 °C

반응 단계

5-Bromo-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acid (CAN 1211586-75-2; 1.5 g; 5.0 mmol) was dissolved in toluene (35 mL) an DMF (2 mL). To this solution was added 1,1′-bis(diphenylphosphino)-ferrocene-palladium(II)dichloride dichloromethane complex (204 mg, 250 μmol), followed by 3-chloro-4-fluorophenylboronic acid (CAN 144432-85-9; 959 mg, 5.5 mmol) and 2M—Na2CO3 (20.0 ml, 40.0 mmol). The reaction mixture was heated to 90° C. and stirred for 4 h, cooled and poured into 100 mL ice water, acidified with 45 mL 2N—HCl and extracted ethyl acetate. The organic layers were combined, dried with Na2SO4 and concentrated in vacuo. The crude material was crystallized from heptane:ethyl acetate (5:1) to yield 1.1 g (63%) of the title compound as light grey solid; LC-MS (UV peak area/ESI): 97%, 348.0066 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729105B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-1594cc1689c24116879ad165bd283b5f
출처 메모uspto-grants-2014_05