HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957271Generated: October 27, 2026
Water → 3-Chloro-2-(4-cyano-3-nitrophenyl)-5-trifluoromethylpyridine
https://huagongshe.com/reaction/1957271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Chloro-2-(4-fluoro-3-nitrophenyl)-5-(trifluoromethyl)pyridine | HCID 22114842 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-2-(4-cyano-3-nitrophenyl)-5-trifluoromethylpyridine | HCID 19068752 | — |
Reaction Steps
5.0 g of 3-chloro-2-(4-fluoro-3-nitrophenyl)-5-trifluoromethylpyridine and 1.5 g of potassium cyanide in 50 ml of dimethylformamide were heated at 50° C. for 4 hours and then stirred at 23° C. for 20 hours. The mixture was then poured into 200 ml of water. The aqueous phase was extracted three times with 100 ml of tertbutyl methyl ether each time. The combined organic phases were washed twice with 50 ml of water each time, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate=9:1). Yield: 2.7 g (53%) of a yellow oil which slowly crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05783522 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-6ede41fbbc33493494ca78ea9791b82c |
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| Source note | uspto-grants-1998_07 |
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