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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2165526Erstellt: 26. Oktober 2026

Benzenesulfonyl chloride → 4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-one

https://huagongshe.com/reaction/2165526

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktPotassium CarbonateHCID 11430—
Edukt2(1H)-Quinoxalinone, 3,4-dihydro-HCID 185949—
LösungsmittelAcetoneHCID 180—
Produkt4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-oneHCID 109323752%

Reaktionsschritte

A suspension of 10 g. (0.068 mole) of 3,4-dihydro-2(1H)-quinoxalinone (3,4-dihydro-2-hydroxyquinoxaline) [prepared in 50% yield according to the procedure described by W. H. Perkin et al. in the Journal of the Chemical Society, Vol. 123, p.2399(1923)] and 9.6 g. (0.069 mole) of potassium carbonate in 250 ml. of acetone was stirred under a nitrogen atmosphere at 40° C., while 11.5 g. (0.07 mole) of benzenesulfonyl chloride was added during the course of a 30-minute period. The reaction mixture was next heated at reflux temperature for 14 hours and then poured onto 500 ml. of ice. The resulting brown solid was recrystallized from ethyl acetate to yield 10.2 g (52%) of pure 4-benzenesulfonyl-3,4-dihydro-2(1H)-quinoxalinone, m.p. 183°-185° C. The pure product was further characterized by means of nuclear magnetic resonance data and elemental analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04940708
Quelldatensatzuspto-grants-1990_07
ORD IDord-e63bd5bf0967443388cb193dc309b8b9
Quellennotizuspto-grants-1990_07