Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277875Generated: October 27, 2026

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

https://huagongshe.com/reaction/277875

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 gray 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 numberUS06358948B1
Source datasetuspto-grants-2002_03
ORD IDord-05b9b20ce0d14d508264f927603049c1
Source noteuspto-grants-2002_03