戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 55857作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物DiisopropylethylamineHCID 81531—
反応物5-Bromo-2-fluoropyridineHCID 2783168—
反応物ButyllithiumHCID 178418339—
生成物5-Bromo-2-fluoro-3-pyridinecarboxaldehydeHCID 4548019262%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09433622B2
出典データセットuspto-grants-2016_09
ORD IDord-c1cf5b7f0b104b03b3d7a995d7afad52
出典メモuspto-grants-2016_09