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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424299Generated: October 31, 2026

Sodium Fluoride → 4-Methoxy-3-(2-methylphenoxy)-6-vinylpyridazine

https://huagongshe.com/reaction/2424299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
ReactantEthyl AcetateHCID 8857—
ReactantTributylvinyltinHCID 81998—
Reactant6-Chloro-4-methoxy-3-(2-methylphenoxy)pyridazineHCID 22940136—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-Methoxy-3-(2-methylphenoxy)-6-vinylpyridazineHCID 2301408988.6%

Reaction Steps

In toluene (2 mL) was dissolved 123 mg (0.490 mmol) of 6-chloro-4-methoxy-3-(2-methylphenoxy)pyridazine obtained in Example 2 (1), 246 mg (0.776 mmol) of tributyl(vinyl) tin, and then, 119 mg (0.103 mmol) of tetrakis(triphenylphosphine)palladium were successively added to the solution at room temperature, and the resulting mixture was refluxed for 3 hours. The reaction mixture was allowed to stand for cooling, ethyl acetate (5 mL), water (3 mL) and sodium fluoride were added to the mixture, and the resulting mixture was stirred for 30 minutes and allowed to stand at room temperature overnight. The mixture was filtered through Celite, ethyl acetate was added to the filtrate, then the organic layer was separated and washed with brine. After drying over anhydrous sodium sulfate, the solvent was removed. The obtained residue was purified by silica gel column chromatography (eluted with hexane:ethyl acetate=1:2) to obtain 105 mg (0.434 mmol, Yield: 88.6%) of 4-methoxy-3-(2-methylphenoxy)-6-vinylpyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964531B2
Source datasetuspto-grants-2011_06
ORD IDord-240f5794aef6411b96a115fc5b6726ba
Source noteuspto-grants-2011_06