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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14933Generated: October 25, 2026

Water → 3-(2-Fluoro-pyridin-4-yl)-benzaldehyde

https://huagongshe.com/reaction/14933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-iodopyridineHCID 7023570—
ReactantFormylphenylboronic acidHCID 66687538—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Fluoro-pyridin-4-yl)-benzaldehydeHCID 86603317—

Reaction Steps

2 fluoro-4-iodo pyridine (5 g), 3 formylphenylboronic acid (4 g), and palladium tetrakis triphenylphosphine were suspended in 500 mL of THF. Potassium carbonate (7.42 g) was added along with 50 mL of water. The flask was purged with nitrogen and the mixture heated to 65 C for 4 hours. The solvent was removed by rotary evaporation and the residue partitioned between ethyl acetate and water. Removal of the ethyl acetate gave a residue which was chromatographed on silica gel (1:1 ethyl acetate hexanes) to give the desired product. Yield: 1.42 g. LC-MS showed the product had the expected M+H+ of 202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732444B2
Source datasetuspto-grants-2010_06
ORD IDord-ca97ba8058b64914b78c231d37fd98b7
Source noteuspto-grants-2010_06