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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1909148생성일: 2026년 10월 25일

Diisopropylamine → Ethyl 5-(2-fluoro-4-methylphenyl)nicotinate

https://huagongshe.com/reaction/1909148

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Ethyl 5-bromopyridine-3-carboxylateHCID 140785—
반응물Sodium BicarbonateHCID 516892—
반응물(2-Fluoro-4-methylphenyl)boronic acidHCID 2783132—
반응물Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물Ethyl 5-(2-fluoro-4-methylphenyl)nicotinateHCID 67338384102.1%

반응 조건

온도80 °C

반응 단계

To a solution of ethyl 5-bromonicotinate (0.58 g, 2.53 mmol) in acetonitrile (15 mL) and water (5 mL) were added (2-fluoro-4-methylphenyl)boronic acid (0.47 g, 3.04 mmol), 3,3′,3″-phosphinidynetris(benzenesulfonic acid) trisodium salt (0.22 g, 0.38 mmol), palladium(II)acetate (28.4 mg, 0.13 mmol) and diisopropylamine (0.90 mL, 6.32 mmol). The mixture was heated to 80° C. After 1 h, the mixture was cooled to ambient temperature and saturated aqueous NaHCO3 was added. The mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→70% hexanes/ethyl acetate) gave the title compound (0.67 g). MS 260.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598209B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-394117abaf164211983341ba147be7a0
출처 메모uspto-grants-2013_12