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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602082Generated: October 25, 2026

Potassium Carbonate → 6-(3-Fluorophenyl)nicotinic acid

https://huagongshe.com/reaction/602082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloronicotinic acidHCID 79222—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product6-(3-Fluorophenyl)nicotinic acidHCID 2472997297.8%

Reaction Steps

3-Fluorophenylboronic acid (39.5 g, 0.282 mol), a solution of K2CO3 (150 g) in water (700 mL), [Bu4N]Br (3.5 g, 0.0107 mol), and Pd(PPh3)4 (12.4 g, 0.0107 mol) were added to a solution of 6-chloronicotinic acid (37.0 g, 0.235 mol) in toluene. The reaction mixture was stirred under reflux for 20 h. After cooling, the reaction mixture was filtered and acidified with 2 M HCl to pH 3. The formed precipitate was separated by filtration and dried to give 6-(3-fluorophenyl)nicotinic acid (yield 97%, 49.9 g). 1H NMR (400 MHz, DMSO-d6) □ ppm 7.29 (td, J=8.46, 2.42 Hz, 1H) 7.50-7.56 (m, 1H) 7.93 (dd, J=10.47, 2.15 Hz, 1H) 7.97 (d, J=7.79 Hz, 1H) 8.11 (d, J=8.06 Hz, 1H) 8.30 (dd, J=8.32, 2.15 Hz, 1H) 9.11 (d, J=1.88 Hz, 1H), 13.48 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902373B2
Source datasetuspto-grants-2011_03
ORD IDord-b4e01c5ab1ff4d6098162f58ac358dca
Source noteuspto-grants-2011_03