Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2040932Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-[2-(4-Chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-one

https://huagongshe.com/reaction/2040932

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAmmonium ChlorideHCID 25517—
EduktPotassium borohydrideHCID 4192641—
Edukt3-(2-(4-Chlorophenoxy)phenyl)-1-methylpyrrolidine-2,4-dioneHCID 23148658—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-[2-(4-Chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-oneHCID 6797973189,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

5 g (15.8 mmol) of 3-[2-(4-chlorophenoxy)phenyl]-1-methylpyrrolidine-2,4-dione (compound IVb) was dissolved in a mixture of 150 mL of tetrahydrofuran and 15 mL of water. The solution was cooled to 0° C., and 4.3 g of potassium borohydride were added slowly, keeping the temperature below 10° C. The resulting solution was stirred at 0° C. for 6 hours. Then, a saturated solution of ammonium chloride was added, and the pH was adjusted to 3 with HCl 2 M. 100 mL of ethyl acetate were added. The organic phase was extracted, washed with saturated sodium bicarbonate and with water, dried and concentrated under vacuum, to obtain 4.5 g of 3-[2-(4-chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-one (compound XIIIb) as a sticky solid. Yield: 89.6%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08580972B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-d3b23bfebb624a09bb92814f10e4d986
Quellennotizuspto-grants-2013_11