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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212606생성일: 2026년 10월 27일

Potassium Carbonate → 2,5-Difluoro-4-methoxy-3-(1,4,4,6-tetramethyl-2-oxo-1,2,3,4-tetrahydro-quinolin-7-yl)-benzaldehyde

https://huagongshe.com/reaction/2212606

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Bromo-2,5-difluoro-4-methoxybenzaldehydeHCID 21966431—
반응물1,4,4,6-tetramethyl-7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinoline-2-oneHCID 21966467—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2,5-Difluoro-4-methoxy-3-(1,4,4,6-tetramethyl-2-oxo-1,2,3,4-tetrahydro-quinolin-7-yl)-benzaldehydeHCID 21966466—

반응 단계

A mixture of 1,4,4,6-tetramethyl-7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinoline-2-one (0.36 g, 1.1 mmol), 3-bromo-2,5-difluoro-4-methoxybenzaldehyde (example 13 a) (0.25 g, 0.1 mmol) and potassium carbonate (0.275 g, 1.99 mmol) in toluene (5 mL), ethanol (1 mL) and water (0.75 mL) was degassed with argon for 30 minutes. Tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.05 mmol) was added and the mixture heated at reflux under argon for 20 hrs. The solution was cooled to room temperature, diluted with ethyl acetate and washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was purified on silica gel (0%–20% ethyl acetate in hexane) to give 97 mg of 2,5-Difluoro-4-methoxy-3-(1,4,4,6-tetramethyl-2-oxo-1,2,3,4-tetrahydro-quinolin-7-yl)-benzaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07102000B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-d2d5e6a394c041c89ee0859a93a0cc5d
출처 메모uspto-grants-2006_09