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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38121Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt1-Pentene, 5-bromo-HCID 70704—
EduktPhthalimide potassium saltHCID 24194345—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(pent-4-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 33943487,9%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524689B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-562ad9d5744848ac81f7bdd9619a6887
Quellennotizuspto-grants-2013_09