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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233206Generated: October 27, 2026

Water → 3-ethenyl-6,7-dihydro-5H-pyrano[2,3-c]pyridazine

https://huagongshe.com/reaction/2233206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant6,7-dihydro-5H-pyrano[2,3-c]pyridazin-3-yl trifluoromethanesulfonateHCID 86614150—
CatalystHCID 178418397HCID 178418397—
Product3-ethenyl-6,7-dihydro-5H-pyrano[2,3-c]pyridazineHCID 6752682577%

Reaction Steps

Argon was bubbled for 15 minutes through a solution of 6,7-dihydro-5H-pyrano[2,3-c]pyridazin-3-yl trifluoromethanesulfonate (228 mg, 0.8 mmol) in 1,2-dimethoxyethane (6.5 ml). Tetrakis(triphenylphosphine)palladium(0) (50 mg, 0.0435 mmol) was added and the solution stirred for 20 minutes under argon. The mixture was then treated with potassium carbonate (111 mg, 0.8 mmol), water (1.9 ml) and triethenylboroxin pyridine complex (180 mg, 0.75 mmol). After stirring for 2 hours at 80° C., the mixture was cooled and partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The layers were separated and the aqueous fraction was extracted twice with 20% methanol/dichloromethane. The combined organic solution was dried, evaporated and the residue chromatographed on silica, eluting with ethyl acetate to give the product as a white solid (100 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709483B2
Source datasetuspto-grants-2010_05
ORD IDord-3338199d6b16410eaa4aa82fc59abe2a
Source noteuspto-grants-2010_05