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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300120Generated: November 3, 2026

Potassium Carbonate → 6-(3-fluorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-one

https://huagongshe.com/reaction/2300120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 10729589—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product6-(3-fluorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-oneHCID 9943324—

Reaction Steps

Prepared by coupling 3-fluorophenylboronic acid with an equivalent amount of 6-bromo-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one using a catalytic amount of tetrakis(triphenylphosphine)palladium(0) with overnight refluxing in toluene containing an equivalent amount of potassium carbonate dissolved in water. Work up in the usual manner followed by recrystallization from ethanol gave a grey solid: mp 190-192° C. 1H-NMR (DMSO-d6) δ 10.27 (s, 1H), 7.57 (s, 1H), 7.50 (m, 4H), 7.15 (m, 1H), 6.95 (d, 1H J=8.2 Hz), 2.39 (s, 2H), 1.29 (s, 6H); MS (APCI (−)) m/z 268 [M−H]− Anal. Calc. For C17H16FNO 0.25 H2O: C, 74.57, H, 6.07, N, 5.12. Found: C, 74.86, H, 5.97, N 5.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498154B1
Source datasetuspto-grants-2002_12
ORD IDord-bfd8fba8860a467597b691a77f7a2032
Source noteuspto-grants-2002_12