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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545295Generated: October 29, 2026

1,1'-Difluoro-2,2'-bipyridinium Bis(tetrafluoroborate) → 5-Fluoro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/545295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Difluoro-2,2'-bipyridinium Bis(tetrafluoroborate)HCID 2733931—
Reactant2,2-Dimethyl-5-(1-hydroxy-3-methylamino-2-butenylidene)-1,3-dioxane-4,6-dioneHCID 76168957—
SolventAcetonitrileHCID 6342—
Product5-Fluoro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylic acidHCID 57672122108.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

1.0 g of 2,2-dimethyl-5-(1-hydroxy-3-methylamino-2-butenylidene)-1,3-dioxane-4,6-dione was suspended in 20 ml of acetonitrile, 806 mg of N,N′-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) was added thereto, and this was stirred at room temperature for 1 hour and at 50° C. for 30 minutes. The reaction mixture was added to 100 ml of ice water and extracted with 100 ml of chloroform twice. The organic layer was dried with anhydrous magnesium sulfate and concentrated, and the residue was subjected to silica gel column chromatography (eluent: ethyl acetate) to obtain 480 mg of 5-fluoro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylic acid represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935716B2
Source datasetuspto-grants-2011_05
ORD IDord-0a4b711149524e739bea5aaf3afcb428
Source noteuspto-grants-2011_05