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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 733216Erstellt: 25. Oktober 2026

N-Ethylphthalimide → 2-ethyl-3-hydroxy-1,3-dihydro-2H-isoindol-1-one

https://huagongshe.com/reaction/733216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-EthylphthalimideHCID 21120—
LösungsmittelMethanolHCID 887—
LösungsmittelPotassium borohydrideHCID 4192641—
Produkt2-ethyl-3-hydroxy-1,3-dihydro-2H-isoindol-1-oneHCID 1530591047%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

3-Hydroxy-2-ethyl-2,3-dihydroisoindol-1-one is prepared as described in Example 1, starting with 4.0 g of N-ethylphthalimide in 20 cm3 of methanol and 1.2 g of potassium borohydride. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours and is then cooled to a temperature in the region of 0° C. and distilled water is added dropwise. The precipitate obtained is filtered off and then washed with cold water. The methanol is then partially evaporated from the filtrate under reduced pressure (2 kPa) at a temperature in the region of 35° C., and the residue is cooled to 0° C. The second precipitate thus obtained is filtered off and then washed with cold water. The two fractions of solid are dried under reduced pressure (2 kPa) at a temperature in the region of 35° C. 1.9 g of 3-hydroxy-2-ethyl-2,3-dihydroisoindol-1-one are thus obtained in the form of a flaky white powder. (Rf=0.5, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (30/70 by volume)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07589117B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-7539f4e08ff74215a8cb335e7b8b9f2b
Quellennotizuspto-grants-2009_09