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HRID 2212579Erstellt: 26. Oktober 2026

Water → 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one

https://huagongshe.com/reaction/2212579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktPotassium HydroxideHCID 14797—
Edukt7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966423—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966429101,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of powdered KOH (14.06 g, 0.250 mol) in DMSO (150 mL) was stirred at 0° C. for 10 min. 7-Bromo-4,4,6-trimethyl-3,4- dihydro-1H-quinoline-2-one (33.59 g, 0.125 mol) was added cautiously, followed immediately by the addition of methyl iodide (39 mL, 0.625 mol). The reaction mixture was kept at 0° C. for 30 min then slowly warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (MgSO4), filtered and evaporated to give 35.74 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one (99%) and used without further purification in the Suzuki coupling (step a). 1H NMR (300 MHz; CDCl3): 1.27 (s, 6 H), 2.37 (s, 3 H), 2.48 (s, 2 H), 3.35 (s, 3 H), 7.12 (s, 1 H), 7.16 (s, 1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07102000B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-831371cfd739469e9a970254baefab82
Quellennotizuspto-grants-2006_09