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HRID 15266作成日:2026年10月27日

Sodium hydride → 5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione

https://huagongshe.com/reaction/15266

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-Methyloxybenzyl chlorideHCID 69993—
反応物5-FluoroisatinHCID 236566—
溶媒DimethylformamideHCID 6228—
生成物5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dioneHCID 767710082.4%

反応手順

A solution of 5-fluoroisatin (5 g, 30.2 mmol) in DMF (60 mL) was cooled in an ice/water bath and treated with sodium hydride (1.44 g, 60.6 mmol) portionwise. The reaction was stirred for 15 minutes after the addition of the last portion and then treated with p-methoxybenzyl chloride (5.32 g, 45.3 mmol) and allowed to stir for 1 hour. The reaction was then quenched by slow addition of excess methanol. After bubbling had stopped, the reaction was poured into water (100 mL) and extracted twice with ethyl acetate. The organics were combined, dried over MgSO4 and the solvent was removed. The residue was purified by silica gel chromatography using a gradient of 0-100% ethyl acetate in hexane to afford 7.1 g (82%) of 5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione; 1H NMR (CDCl3, 400 MHz) δ 3.79 (s, 3H), 4.86 (s, 2H), 6.75 (dd, 1H, J1=3.6, J2=8.6), 6.84-6.90 (m, 2H), 7.19 (ddd, 1H, J1=J2=8.6, J3=3.6), 7.22-7.27 (m, 1H), 7.26-7.31 (m, 2H); HPLC-MS calcd. for C16H12FNO3 (M+H+) 286.1, found 286.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732449B2
出典データセットuspto-grants-2010_06
ORD IDord-99fd54b087c9445395ee3f31e753d922
出典メモuspto-grants-2010_06