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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602097생성일: 2026년 10월 25일

2-Fluorophenylboronic acid → Tert-butyl 6-(2-fluorophenyl)nicotinate

https://huagongshe.com/reaction/602097

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참여 물질

역할이름HCID투입량
반응물2-Fluorophenylboronic acidHCID 2734354—
반응물(tert-Butyl) 6-bromonicotinateHCID 26369925—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
생성물Tert-butyl 6-(2-fluorophenyl)nicotinateHCID 6726799542.2%

반응 조건

온도90 °C

반응 단계

To a round-bottom flask was added 2-fluoro phenylboronic acid (271 mg, 1.94 mmol), palladium tetrakis(triphenylphosphine) (22.4 mg, 0.0194 mmol)) and tert-butyl 6-bromonicotinate (500 mg, 1.94 mmol) and the mixture was evacuated 3× with N2. The solids were dissolved in 25 mL of DMF, followed by addition of 2.9 mL of 2 M cesium carbonate. The resulting mixture was heated to ˜90° C. The mixture was cooled to room temperature and then poured into a seperatory funnel, followed by addition of EtOAc and water (1×200 mL). The layers were separated and the organic extract washed with brine (1×200 mL), dried MgSO4, filtered and concentrated to afford an orange oil. The crude mixture was purified by chromatography (silica, 10% EtOAc:Heptane) to afford the desired product (224 mg, 40%). 1H NMR (400 MHz, DMSO-d6) □ ppm 9.16 (1H, d, J=2.2 Hz), 8.34 (1H, dd, J=8.3, 2.3 Hz), 7.90-8.05 (2H, m), 7.50-7.62 (1H, m), 7.33-7.44 (2H, m) 1.59 (9 H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902373B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-be25294b13c34883baf5e1c4cbf140ff
출처 메모uspto-grants-2011_03