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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554636Generated: October 30, 2026

Potassium Carbonate → [5-(4-Fluoro-2-formyl-phenyl)-pyridin-3-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/554636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(5-bromopyridin-3-yl)acetateHCID 54116619—
Reactant5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehydeHCID 59420279—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product[5-(4-Fluoro-2-formyl-phenyl)-pyridin-3-yl]-acetic acid ethyl esterHCID 58565095—

Reaction Conditions

Temperature75 °C

Reaction Steps

(5-Bromo-pyridin-3-yl)-acetic acid ethyl ester (1.91 g, 7.8 mmol), 5-fluoro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehyde (50% pure; 2.94 g, 11.75 mmol), and potassium carbonate (3.25 g, 23.5 mmol) were combined in 2:1 DME:H2O, and the solution was purged with N2 for 20 minutes. Tetrakis(triphenylphosphine)palladium(0) (0.45 g, 0.39 mmol) was added, and the reaction was purged with N2 for another 25 minutes and then stirred at 75° C. for 2 hours. The mixture was worked up with EtOAc and H2O, and the residue was purified by silica gel chromatography (0-100% EtOAc in hexanes) to give [5-(4-fluoro-2-formyl-phenyl)-pyridin-3-yl]-acetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049015B2
Source datasetuspto-grants-2011_11
ORD IDord-41f391aefce24c35ba710f90ff5ed887
Source noteuspto-grants-2011_11