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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15179Generated: October 26, 2026

Water → 3-Ethenyl-5,6-dihydrofuro[2,3-c]pyridazine

https://huagongshe.com/reaction/15179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
Reactant5,6-Dihydrofuro[2,3-c]pyridazin-3-yl trifluoromethanesulfonateHCID 86614156—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Ethenyl-5,6-dihydrofuro[2,3-c]pyridazineHCID 67527357—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 5,6-dihydrofuro[2,3-c]pyridazin-3-yl trifluoromethanesulfonate (500 mg, 1.85 mmol) in dimethoxyethane (20 ml) was degassed then treated with tetrakis(triphenylphosphine)palladium (0) (116 mg), potassium carbonate (257 mg), 2,4,6-trivinylcyclotriboroxane pyridine complex (for a preparation of this reagent see F. Kerins and D. F. O'Shea, J. Org. Chem. 2002, 67, 4968-4971) (416 mg) and water (3.6 ml). The mixture was stirred at 80° C. for 2 hours then partitioned between DCM and saturated aqueous sodium bicarbonate solution. The aqueous phase was extracted with 10% methanol in DCM then the combined organic extracts dried and evaporated. The residue was chromatographed eluting with ethyl acetate affording a white solid (111 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732460B2
Source datasetuspto-grants-2010_06
ORD IDord-bec46baf34f44f1f884d7e5c93337c07
Source noteuspto-grants-2010_06