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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120750Generated: October 30, 2026

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

https://huagongshe.com/reaction/2120750

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-dihydo-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 (r, 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 0.25H2O: 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 numberUS06693103B2
Source datasetuspto-grants-2004_02
ORD IDord-460276a5092a4f4f86425092b02ae437
Source noteuspto-grants-2004_02