HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908581Generated: October 30, 2026
Potassium Cyanide → HCID 11998318, compound
https://huagongshe.com/reaction/908581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | HCID 86637146 | HCID 86637146 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 11998318 | HCID 11998318 | — |
Reaction Steps
2-Bromo-6-(3-pyridin-3-yl-[1,2,4]oxadiazol-5-yl)-pyridine (250 mg, 0.83 mmol) and 80 mg of potassium cyanide (1.24 mmol) in 15 ml of acetonitrile was degassed three times (vacuum/nitrogene), added a solution of 24 μl Tributyltin chloride (1 μmol) in heptane, 2.3 mg of bis-(diphenylphosphino)ferrocene (4.1 μmol) and 4 mg of bispalladium tris(dibenzylidene acetone) (4.1 μmol) were added. The suspension was degassed three times and stirred at ambident temperature for 30 minutes. The mixture was degassed again and heated at 80° C. for 17 hours. The reaction mixture concentrated, residue was diluted with ethyl acetate and washed with water. The organic layer was dried with sodium sulphate, concentrated, and purified by column chromatography over silica gel using 20% ethyl acetate in petroleum ether, Yield 80 mg. Mp 201-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017631B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-e5015aa5a6ba470081a7c22f30662580 |
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| Source note | uspto-grants-2011_09 |
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