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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1630744생성일: 2026년 10월 26일

Potassium Carbonate → 3-Methoxy-6-methyl-2-(4-(trifluoromethyl)phenyl)pyridine

https://huagongshe.com/reaction/1630744

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
반응물2-Iodo-3-methoxy-6-methylpyridineHCID 11482051—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물3-Methoxy-6-methyl-2-(4-(trifluoromethyl)phenyl)pyridineHCID 58443268—

반응 조건

온도75 °C

반응 단계

To a mixture of 4-(trifluoromethyl)phenylboronic acid (0.97 g, 5.1 mmol), S—PHOS (0.20 g, 0.47 mmol), potassium carbonate (2.0 g, 15 mmol), and Pd(OAc)2 (0.061 g, 0.27 mmol) was added a solution of 2-iodo-3-methoxy-6-methylpyridine (prepared in the previous step) in acetonitrile (6 mL) followed by water (4 mL). The reaction mixture was degassed by bubbling nitrogen through the solution for 10 min, and the reaction mixture was heated to 75° C. After 4 h, the reaction mixture was diluted with EtOAc, washed with saturated NaHCO3 (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (5% to 20% EtOAc in hexanes) gave 3-methoxy-6-methyl-2-(4-(trifluoromethyl)phenyl)pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791147B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-0efef0adc9b44a178b643bef49bc58a1
출처 메모uspto-grants-2014_07