HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467042Generated: October 26, 2026
Potassium Carbonate → 2-(3-Phenoxyphenoxy)-3-cyanopyridine
https://huagongshe.com/reaction/467042
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Phenoxyphenol | HCID 12842 | — |
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Phenoxyphenoxy)-3-cyanopyridine | HCID 19771889 | 157% |
Reaction Steps
A mixture of potassium carbonate (5.53 g, 0.04 mol) and 3-phenoxyphenol (15 g, 0.08 mol) in DMF (60 ml) was heated at 80° C. with stirring for 30 minutes. 2-Chloro-3-cyanopyridine (11.08 g, 0.08 mol) and copper bronze (0.8 g) were added and the resulting mixture heated at reflux for 90 minutes. GC analysis indicated the formation of a single product (96%). The reaction mixture was cooled and filtered, and then poured into water (300 ml) and allowed to stand over the weekend. The yellow-brown oily precipitate was extracted into dichloromethane and dried. The dichloromethane solution was then filtered and evaporated to yield crude 2-(3-phenoxyphenoxy)-3-cyano-pyridine (36.2 g, contaminated with DMF) which was used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158954 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-b50908ce498541fd8ad711932b7cfabf |
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| Source note | uspto-grants-1992_10 |
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