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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638995Generated: November 1, 2026

Potassium Carbonate → 4-Ethenyl-3,8-difluoro-6-methoxyquinoline

https://huagongshe.com/reaction/638995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3,8-difluoro-6-methoxyquinolineHCID 68576832—
ReactantHCID 178419161HCID 178419161—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Ethenyl-3,8-difluoro-6-methoxyquinolineHCID 5902609290%

Reaction Steps

4-Bromo-3,8-difluoro-6-(methoxy)quinoline (0.63 g, 2.3 mmol) in DME (26 mL) under argon, was treated with tetrakis(triphenylphosphine)palladium(0) (0.13 g, 0.115 mmol) and the mixture stirred at room temperature for 20 minutes. Anhydrous potassium carbonate (0.32 g, 2.3 mmol), water (7 mL), and vinylborane:pyridine complex (see F. Kerins and D O'Shea J. Org. Chem. 2002, 67, 4968-4971) (0.22 g, 0.92 mmol) were added and the mixture was heated at 100° C. for 2 hr. It was cooled, diluted with water and extracted with ether, dried over magnesium sulfate and evaporated to dryness. After work-up the product was chromatographed on silica gel, eluting with 10% methanol in DCM to afford a white solid (0.46 g, 90%). MS (+ve ion electrospray) m/z 221 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691850B2
Source datasetuspto-grants-2010_04
ORD IDord-6d85d8f564a74eefa82a3f5dc902e62a
Source noteuspto-grants-2010_04