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HRID 38121作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物1-Pentene, 5-bromo-HCID 70704—
反応物Phthalimide potassium saltHCID 24194345—
溶媒DimethylformamideHCID 6228—
生成物2-(pent-4-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 33943487.9%

反応条件

温度100 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524689B2
出典データセットuspto-grants-2013_09
ORD IDord-562ad9d5744848ac81f7bdd9619a6887
出典メモuspto-grants-2013_09