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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20747Erstellt: 23. Oktober 2026

N-Hydroxyphthalimide → Ethyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoate

https://huagongshe.com/de/reaction/20747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-HydroxyphthalimideHCID 10665—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 4-bromobutyrateHCID 76300—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoateHCID 10850119100%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 4-bromo-n-butyric acid ethyl ester (1.2 g, 6.13 mmol) in dimethylformamide (9 ml) were added N-hydroxyphthalimide (1.5 g, 9.19 mmol) and Hunig base (N,N-diisopropylethylamine, 2.13 mL) at room temperature, and the mixture was stirred at 80° C. over night. The reaction mixture was poured into saturated aqueous ammonium chloride, and the resultant mixture was extracted with ethyl acetate (3×40 ml). The combined organic layers were washed with saturated brine (2×30 ml), dried over Na2SO4, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (100 g, n-hexane/ethyl acetate (2:1)) to give 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester (1.47 g, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745663B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3f4a91da137348fab27f70c6fd15f396
Quellennotizuspto-grants-2010_06