돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15266생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/15266

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Methyloxybenzyl chlorideHCID 69993—
반응물5-FluoroisatinHCID 236566—
용매DimethylformamideHCID 6228—
생성물5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dioneHCID 767710082.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732449B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-99fd54b087c9445395ee3f31e753d922
출처 메모uspto-grants-2010_06