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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Trivinylboroxin-Pyridine Complex | HCID 2734806 | — |
| Reactant | 5,6-Dihydrofuro[2,3-c]pyridazin-3-yl trifluoromethanesulfonate | HCID 86614156 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-Ethenyl-5,6-dihydrofuro[2,3-c]pyridazine | HCID 67527357 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732460B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-bec46baf34f44f1f884d7e5c93337c07 |
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| Source note | uspto-grants-2010_06 |
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