Реакция #155400
ord-968a86666c514b66ad2f8f26e08fb3e7
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe reaction mixture was cooled to room temperature
- 2ЭкстракцияThe aqueous layer was then extracted with ethyl acetate (2×50 mL)
- 3Промывкаthe combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL)
- 4Сушкаdried over Na2SO4
- 5ФильтрацияFiltration and solvent evaporation
- 6Другоеgave an oil, which
- 7Другоеwas purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-35%)
Методика
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, 4H), 5.70-5.91 (m, 1H), 4.90-5.11 (m, 2H), 3.58 (t, 2H), 1.98-2.10 (m, 2H), 1.59-1.78 (m, 2H).