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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 424070생성일: 2026년 10월 25일

Potassium Iodide → 2-(4-Methoxy-benzyl)-4-[2-(2-methoxy-ethoxy)-ethoxy]-isoindole-1,3-dione

https://huagongshe.com/reaction/424070

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-Bromo-3,6-dioxaheptaneHCID 123532—
반응물4-Hydroxy-2-(4-methoxy-benzyl)-isoindole-1,3-dioneHCID 59263145—
용매DimethylformamideHCID 6228—
생성물2-(4-Methoxy-benzyl)-4-[2-(2-methoxy-ethoxy)-ethoxy]-isoindole-1,3-dioneHCID 5926313373%

반응 조건

온도60 °C

반응 단계

1-(2-Bromo-ethoxy)-2-methoxy-ethane (107 mg, 0.58 mmol) was added to a suspension of 4-hydroxy-2-(4-methoxy-benzyl)-isoindole-1,3-dione (150 mg, 0.53 mmol) and potassium carbonate (200 mg, 1.4 mmol) in DMF (2 mL). After 3.5 hours, a catalytic amount of potassium iodide was added. After a further 17 hours, the mixture was warmed to 60° C. After 3 hours, an additional amount of 1-(2-bromo-ethoxy)-2-methoxy-ethane (20 mg, 0.11 mmol) was added and the mixture maintained at 60° C. for a further 20 hours. The mixture was concentrated in vacuo then the residue was taken up in ethyl acetate and washed with potassium carbonate solution and brine. The organic phase was dried (MgSO4) and concentrated to give the title compound as a yellow oil (149 mg, 73%). 1H NMR (methanol-d4) 7.71 (1H, t), 7.43-7.40 (2H, m), 7.31-7.27 (2H, m), 6.87-6.83 (2H, m), 4.71 (2H, s), 4.37-4.34 (2H, m), 3.92-3.89 (2H, m), 3.77-3.74 (5H, m), 3.55-3.53 (2H, m), 3.33 (3H, s). MS: [M+H]+ 386.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101648B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-4feb1e3461ec43f992f2ffda74a3a886
출처 메모uspto-grants-2012_01