Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33381Erstellt: 25. Oktober 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Acetyl-7-(benzyloxy)quinolin-2(1H)-one

https://huagongshe.com/reaction/33381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Edukt5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-oneHCID 21072850—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-Acetyl-7-(benzyloxy)quinolin-2(1H)-oneHCID 21072849—

Reaktionsschritte

13.0 g (44 mmol) 5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-one are suspended in 130 mL dioxane and combined with 15.0 g (66 mmol) of 2,3-dichloro-5,6-dicyanobenzoquinone. The mixture is refluxed for 30 minutes, cooled to ambient temperature and stirred for a further 2 hours. The solid is filtered off, washed with dioxane and dissolved in 600 mL dichloromethane/methanol (9:1). The solution is washed with sodium hydrogen carbonate solution, dried with sodium sulphate and evaporated down. Then the residue is suspended in methanol, filtered and dried.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429583B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-77418d8c43974fee8734f31649c38fcb
Quellennotizuspto-grants-2008_09