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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183981Generated: November 2, 2026

Potassium Acetate → HCID 22329529, compound

https://huagongshe.com/reaction/2183981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(neopentyl glycolato)diboronHCID 2734316—
ReactantHCID 22329485HCID 22329485—
CatalystCID 53485975HCID 53485975—
SolventDimethyl SulfoxideHCID 679—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22329529HCID 22329529—

Reaction Conditions

Temperature85 °C

Reaction Steps

To 2-(5-bromo-2-fluorophenyl)-5-fluoropyridine (0.94 g, 3.48 mmol) and bis(neopentyl glycolato)diborane (0.943 g) in 1,4-dioxane (12 ml) and dimethylsulfoxide (1.5 ml) was added potassium acetate (0.725 g) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (100 mg). The mixture was degassed with nitrogen and then stirred at 85° C. for 15 h. On cooling to ambient temperature, 1N aqueous sodium hydroxide (32 ml) was added and the mixture stirred for 20 min. Diethyl ether was added and the aqueous phase separated and washed with diethyl ether. The organic extracts were washed with water, and the combined aqueous phases filtered then acidified to pH 5 by addition of 2N aqueous hydrochloric acid (18 ml). The resulting white solid was collected by filtration, washed with water and dried in vacuo to afford 4-fluoro-3-(5-fluoropyridin-2-yl)phenylboronic acid: δH (400 MHz, DMSO) 8.73 (1H, dd, J 2 and 1), 8.33 (1H, dd, J 9 and 2), 8.17 (2H, s), 7.87 (3H, m), 7.31 (1H, dd, J 12 and 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-21697f72e47748f4bae67fa11f66b9f1
Source noteuspto-grants-2005_05