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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821686Generated: November 1, 2026

Sodium Fluoride → HCID 23013753, compound

https://huagongshe.com/reaction/1821686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
ReactantEthyl AcetateHCID 8857—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant6-Chloro-4-methoxy-3-(2-methylphenoxy)pyridazineHCID 22940136—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 23013753HCID 2301375314.1%

Reaction Steps

In toluene (6.5 mL) was dissolved 321 mg (1.28 mmol) of 6-chloro-4-methoxy-3-(2-methylphenoxy)pyridazine obtained in Example 2 (1), 534 mg (1.48 mmol) of (1-ethoxyvinyl)(tributyl)tin, then 155.3 mg (0.134 mmol) of tetrakis(triphenylphosphine)palladium were successively added to the solution at room temperature, and the resulting mixture was refluxed for 3 hours and 20 minutes. The reaction mixture was allowed to stand at room temperature overnight, then, ethyl acetate, water and sodium fluoride were added to the mixture and the resulting mixture was stirred for 2 hours. The mixture was filtered through Celite, ethyl acetate was added to the filtrate, and the organic layer was separated, and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was removed. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate, gradient) to obtain 51.8 mg (0.181 mmol, Yield: 14.1%) of 6-(1-ethoxyvinyl)-4-methoxy-3-(2-methylphenoxy)pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-e463b1fadd684163bff933e5f4007af4
Source noteuspto-grants-2009_10