HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619624Generated: October 26, 2026
Cesium fluoride → 3-Pyridazin-4-ylbiphenyl-4-ol
https://huagongshe.com/reaction/1619624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 4-Hydroxy-3-iodobiphenyl | HCID 4106140 | — |
| Reactant | 4-(Tributylstannyl)pyridazine | HCID 6409733 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Pyridazin-4-ylbiphenyl-4-ol | HCID 136200886 | 32% |
Reaction Steps
3-Iodobiphenyl-4-ol (1 g, 3.4 mmol) was mixed with 4-(tributylstannyl)pyridazine (1.25 g 3.4 mmol), caesium fluoride (1.03 g 6.8 mmol), tetrakis(triphenylphosphine) palladium (0) (195 mg, 0.17 mmol) and copper iodide (128 mg 0.68 mmol) in acetonitrile (10 mL). The reaction was degassed 3 times before being placed under nitrogen and heated to 45° C. for 16 hours. The reaction was diluted with acetonitrile (20 mL), washed with heptane (2×20 mL) then absorbed onto silica and purified by silica gel column chromatography (ISCO™, 40 g, 50%-100% ethyl acetate in heptane gradient elution) to afford the title compound (270 mg, 32%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772293B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-20595fd2e1be40208b9753ad19243e68 |
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| Source note | uspto-grants-2014_07 |
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