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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44174Erstellt: 24. Oktober 2026

Ethyl Bromide → 6-Bromo-1-ethyl-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/de/reaction/44174

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
Edukt6-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 14373281—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-Bromo-1-ethyl-3,4-dihydroquinolin-2(1H)-oneHCID 6691130469%

Reaktionsschritte

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (750 mg, 3.32 mmol) in 20 ml dry DMF was added potassium tert-butylate (804 mg, 6.64 mmol). After the mixture was stirred for 30 min at room temperature, a solution of ethyl bromide (724 mg, 6.64 mmol) in 10 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 150 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 1/1, Rf=0.52) gave 6-bromo-1-ethyl-3,4-dihydro-1H-quinolin-2-one (583 mg, 2.29 mmol, 59%) as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541404B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-1ce98bb2e7c3438e8b24f96ce768f4f9
Quellennotizuspto-grants-2013_09