Реакция #155400

ord-968a86666c514b66ad2f8f26e08fb3e7

Уравнение реакции

O
water
C=CCCCBr
5-bromo-pentene
O=C([O-])[O-].[K+].[K+]
K2CO3
O=C1NC(=O)c2ccccc21.[K]
potassium phthalimide
C=CCCCN1C(=O)c2ccccc2C1=O
2-(pent-4-enyl)-isoindoline-1,3-dione
Выход 87.9%

Реагенты

Нет

Растворители

Условия реакции

Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was cooled to room temperature
  2. 2
    ЭкстракцияThe aqueous layer was then extracted with ethyl acetate (2×50 mL)
  3. 3
    Промывкаthe combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL)
  4. 4
    Сушкаdried over Na2SO4
  5. 5
    ФильтрацияFiltration and solvent evaporation
  6. 6
    Другоеgave an oil, which
  7. 7
    Другоеwas 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822424B2uspto-grants-2014_09