戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 671作成日:2026年10月23日

Pyrrolidine → 5-Fluoro-2-(pyrrolidin-1-yl)benzaldehyde

https://huagongshe.com/ja/reaction/671

反応式

関与物質

役割名称HCID仕込み量
反応物PyrrolidineHCID 31268—
反応物2-Bromo-5-fluorobenzaldehydeHCID 2773321—
試薬Cesium carbonateHCID 10796—
触媒Binap, (A+-)-HCID 634876—
触媒Palladium (II) acetateHCID 4144353—
溶媒TolueneHCID 1140—
生成物5-Fluoro-2-(pyrrolidin-1-yl)benzaldehydeHCID 433128910%

反応条件

温度95 °C

反応手順

To a mixture of pyrrolidine (328 mg, 3.05 mmol), 2-bromo-4-fluorobenzaldehyde (619 mg, 3.05 mmol) in toluene (10 ml) was added Cs2CO3 (2.48g, 7.62 mmol), BINAP (95 mg ) and palladium(II) acetate (35 mg) was added. The mixture was purged with Ar for 5 min, then heated at 95 oC for 4 hrs. After cooled to RT, EtOAc (30 mL) was added. The organic layer was washed with water (3 x 30 mL), brine (30 mL), dried over MgSO4, filetred and concentrated. The residue was purified via combiflush (0 - 20% EtOAc/Hexane; 40 g column) to give the desired product as a clear reddish liquid. LCMS and H-NMR look good. 290 mg Conclusion: reaction progressed to give desired product in 49% yield.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-ac71d193208d45949ee247d7a0855249
出典メモ750 AstraZeneca ELN dataset