Carbonic Acid → 5-Chloro-2-(3-fluorophenyl)quinoline-3-carbaldehyde

Participants

Reaction Conditions

Reaction Steps

A mixture of 2,5-dichloroquinoline-3-carbaldehyde (1.0000 g, 4.424 mmol), 3-fluorophenylboronic acid (0.6808 g, 4.866 mmol), tetrakis(triphenylphosphine)-palladium (0.2556 g, 0.2212 mmol), and sodium carbonate anhydrous (2.344 g, 22.12 mmol) in acetonitrile-water (3:1) (0.04000 mL) was stirred at 100° C. After 3 h, the mixture was cooled to room temperature and partitioned between EtOAc (100 mL) and water (100 mL). The organic layer was washed with brine (50 mL×2), dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography on a 80 g of Redi-Sep™ column using 0 to 50% gradient of EtOAc in hexane over 25 min and then 50% isocratic of EtOAc for 10 min as eluent to give 5-chloro-2-(3-fluorophenyl)-quinoline-3-carbaldehyde as a yellow solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 10.14 (1 H, s), 9.06 (1 H, d, J=0.8 Hz), 8.13-8.18 (1 H, m), 7.92-8.00 (2 H, m), 7.59-7.67 (2 H, m), 7.53-7.58 (1 H, m), 7.39-7.47 (1 H, m); LC-MS (ESI) m/z 286.0 [M+H]+.

Provenance & Evidence