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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1943617Erstellt: 25. Oktober 2026

2,7-Dichloroquinoxaline → 7-Chloroquinoxalin-2-amine

https://huagongshe.com/reaction/1943617

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,7-DichloroquinoxalineHCID 2758223—
EduktAmmonia methanolHCID 21705897—
Produkt7-Chloroquinoxalin-2-amineHCID 60166298%

Reaktionsschritte

At T=120° C., 30.0 g (60.0 mmol) of 2,7-dichloroquinoxaline are stirred in 400 ml of NH3/MeOH (w=22%) for 16 hours. The mixture is then evaporated to dryness under reduced pressure, and the residue is taken up in 250 ml of dichloromethane and 250 ml of water. After phase separation, the organic phase is then washed with 250 ml of water and dried over sodium sulphate, and the solvent is removed under membrane pump vacuum. The residue obtained is purified by column chromatography on silica gel (ethyl acetate/petroleum ether=1:5; silica gel: 200-300 mesh), which gives 10.5 g of 7-chloroquinoxalin-2-ylamine (yield 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08394801B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-a8e871c8ce2e4ccc8a3e12610cb0040c
Quellennotizuspto-grants-2013_03