HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054105Generated: November 4, 2026
p-Fluoronitrobenzene → N-(4-Nitrophenyl)pyridin-2-amine
https://huagongshe.com/reaction/2054105
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-(4-Nitrophenyl)pyridin-2-amine | HCID 12695755 | 19.7% |
Reaction Steps
0.3 g of 4-fluoronitrobenzene, 0.4 g of 2-aminopyridine, and 0.353 g of K2CO3 were added to a solution of 2.5 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 1 hour and 0.286 g of potassium tert-butoxide was then added. Heating was then continued for 6 hours and, after cooling to room temperature, the reaction medium was then poured into a water and ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 0.09 g of N-(4-nitrophenyl)pyrid-2-amine (5) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329288B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-04b152c713f746bd990f3f61d0b4e626 |
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| Source note | uspto-grants-2008_02 |
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