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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241581Erstellt: 25. Oktober 2026

Acetone → 7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-one

https://huagongshe.com/reaction/241581

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktPotassium CarbonateHCID 11430—
Edukt1-Bromo-4-chlorobutaneHCID 81364—
Edukt7-Hydroxy-3,4-dihydrocarbostyrilHCID 2785758—
LösungsmittelHexaneHCID 8058—
Produkt7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-oneHCID 1046746778%

Reaktionsschritte

1-bromo-4-chloro-butane (3.4 g, 20 mmol), anhydrous potassium carbonate powder (4.14 g, 30 mmol) and 7-hydroxy-3,4-dihydro-2(1H)-quinolinone (1.63 g, 10 mmol) are added to 10 ml of acetone and reflux for 24 hours. The reaction solution is evaporated to dryness and dispersed with 20 ml of dichloromethane and 20 ml of water respectively. The organic layer is extracted with water (20 ml×2) and saturated saline (20 ml) successively, dried over anhydrous magnesium sulfate, and evaporated to dryness, to obtain a light yellow powder. The resulting powder is slurried with n-hexane (20 ml×3), filtered, and dried to obtain 1.98 g of 7-(4-chlorobutoxy)-3,4-dihydro-2(1H)-quinolinone, with a yield of 78%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653069B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-fb3ae03c07f64429af56703797c27a50
Quellennotizuspto-grants-2014_02