HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340374Generated: October 25, 2026
3,5-Dichloro-2-cyanopyridine → HCID 66874911, compound
https://huagongshe.com/reaction/340374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dichloro-2-cyanopyridine | HCID 2769699 | — |
| Reactant | 1-(4-Ethynylphenyl)ethan-1-one | HCID 5123626 | — |
| Reactant | triethylamine N,N-dimethylformamide | HCID 22056947 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 66874911 | HCID 66874911 | — |
Reaction Steps
To a solution of 1-(4-ethynylphenyl)ethanone (commercially available) (1 eq) 3,5-dichloropicolinonitrile (1 eq), dichlorobis(triphenylphosphine)-palladium (II) (20 mol %), copper iodide (10 mol %) and DMF:Triethylamine (10:1) (0.13 M) was stirred at ambient temperature overnight. The reaction mixture was then diluted with ethyl acetate and sodium bi-carbonate solution. The two phases were separated, and the aqueous phase was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, and concentrated en vacuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane and 5-((4-acetylphenyl)ethynyl)-3-chloropicolinonitrile was isolated as a yellow solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895577B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ab267806ac65428e94eaa7d533628a16 |
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| Source note | uspto-grants-2014_11 |
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