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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38121생성일: 2026년 10월 23일

Water → 2-(pent-4-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dione

https://huagongshe.com/ko/reaction/38121

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1-Pentene, 5-bromo-HCID 70704—
반응물Phthalimide potassium saltHCID 24194345—
용매DimethylformamideHCID 6228—
생성물2-(pent-4-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 33943487.9%

반응 조건

온도100 °C

반응 단계

To a stirring solution of 5-bromo-pentene (6.0 g, 0.040 mol) in DMF (30 mL) was added K2CO3 (4.7 g, 0.034 mol) and potassium phthalimide (6.21 g, 0.033 mmol) and the reaction mixture was heated at 100° C. for 1 hr. The reaction mixture was cooled to room temperature, and water (50 mL) was added. The aqueous layer was then extracted with ethyl acetate (2×50 mL), and the combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL) and dried over Na2SO4. Filtration and solvent evaporation gave an oil, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-35%) to yield the desired 2-(pent-4-enyl)-isoindoline-1,3-dione as a solid (6.36 g, 0.029 mmol, 72.5% yield): MS m/e [M+H]+ calcd 216.1, found 216.1; NMR (250 MHz, DMSO-d6) δ 7.79-7.95 (m, 4 H), 5.70-5.91 (m, 1 H), 4.90-5.11 (m, 2 H), 3.58 (t, 2 H), 1.98-2.10 (m, 2 H), 1.59-1.78 (m, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524689B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-562ad9d5744848ac81f7bdd9619a6887
출처 메모uspto-grants-2013_09