Réaction #155400

Équation de réaction

water

5-bromo-pentene

K2CO3

potassium phthalimide

→

2-(pent-4-enyl)-isoindoline-1,3-dione

Rendement 87.9%

Solvants

DMF

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture was cooled to room temperature
2. 2
   ExtractionThe aqueous layer was then extracted with ethyl acetate (2×50 mL)
3. 3
   Lavagethe combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL)
4. 4
   Séchagedried over Na2SO4
5. 5
   FiltrationFiltration and solvent evaporation
6. 6
   Autregave an oil, which
7. 7
   Autrewas purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-35%)

Mode opératoire

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).

Source