HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927125Generated: November 3, 2026
Potassium Carbonate → HCID 86677037, compound
https://huagongshe.com/reaction/927125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Trivinylboroxin-Pyridine Complex | HCID 2734806 | — |
| Reactant | 3,4-Bis(benzyloxy)-6-chloropyridazine | HCID 12213474 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86677037 | HCID 86677037 | 75.3% |
Reaction Steps
A vessel containing 2,4,6-triethenyl-1,3,5,2,4,6-trioxatriborinane compound with pyridine (1:1) (1.105 g, 4.59 mmol), 3,4-bis(benzyloxy)-6-chloropyridazine (Intermediate 1, 3 g, 9.18 mmol) and potassium carbonate (3.17 g, 22.95 mmol) was evacuated and flushed with nitrogen. Dioxane (30 ml) and water (3 ml) were added in vacuo and the reaction was degassed before tetrakis(triphenyl-phosphine)palladium(0) (0.530 g, 0.459 mmol) was added. The resulting mixture was then heated at 80° C. for 18 hours and upon cooling, was diluted with ethyl acetate and washed with saturated aqueous sodium carbonate solution. The organics were dried (MgSO4), filtered and solvent removed in vacuo to give a brown oil. This was purified by column chromatography (silica, eluting with 0-30% ethyl acetate in petrol) to afford 3,4-bis(benzyloxy)-6-ethenylpyridazine (1.1 g, 38% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290456B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f02c947edb1249b5bdbdf840e95bfb98 |
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| Source note | uspto-grants-2016_03 |
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