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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55857생성일: 2026년 10월 24일

Tetrahydrofuran → 5-Bromo-2-fluoro-3-pyridinecarboxaldehyde

https://huagongshe.com/ko/reaction/55857

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromo-2-fluoropyridineHCID 2783168—
반응물ButyllithiumHCID 178418339—
생성물5-Bromo-2-fluoro-3-pyridinecarboxaldehydeHCID 4548019262%

반응 단계

To a stirred solution of DIPEA (44.1 mL, 312 mmol) in dry THF (500 mL) at −78° C. was added dropwise n-BuLi (2.5M in hexanes, 125 mL, 313 mmol). The temperature was warmed to rt and stirred for 10 minutes. The solution was cooled to −78° C. and a solution of 5-bromo-2-fluoro-pyridine (1) (50.0 g, 284 mmol) in THF (500 mL) added dropwise. The reaction mixture was stirred at −78° C. for 45 minutes then quenched with 10% citric acid in THF (250 mL) at −78° C. The solution was warmed to rt then diluted with H2O (250 mL). The solution was extracted with EtOAc (3×250 mL) and the combined organics washed with saturated brine solution (250 mL), dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by column chromatography (100-200 mesh silica gel, 20% EtOAc-pet ether) to provide the title compound as a white solid (36.0 g, 62%); Rf: 0.7 (10% EtOAc-pet ether).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09433622B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-c1cf5b7f0b104b03b3d7a995d7afad52
출처 메모uspto-grants-2016_09