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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20747생성일: 2026년 10월 24일

N-Hydroxyphthalimide → Ethyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoate

https://huagongshe.com/ko/reaction/20747

반응식

참여 물질

역할이름HCID투입량
반응물N-HydroxyphthalimideHCID 10665—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 4-bromobutyrateHCID 76300—
반응물DiisopropylethylamineHCID 81531—
용매DimethylformamideHCID 6228—
생성물Ethyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoateHCID 10850119100%

반응 조건

온도80 °C

반응 단계

To a solution of 4-bromo-n-butyric acid ethyl ester (1.2 g, 6.13 mmol) in dimethylformamide (9 ml) were added N-hydroxyphthalimide (1.5 g, 9.19 mmol) and Hunig base (N,N-diisopropylethylamine, 2.13 mL) at room temperature, and the mixture was stirred at 80° C. over night. The reaction mixture was poured into saturated aqueous ammonium chloride, and the resultant mixture was extracted with ethyl acetate (3×40 ml). The combined organic layers were washed with saturated brine (2×30 ml), dried over Na2SO4, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (100 g, n-hexane/ethyl acetate (2:1)) to give 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester (1.47 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745663B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3f4a91da137348fab27f70c6fd15f396
출처 메모uspto-grants-2010_06