HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33088Generated: October 25, 2026
p-Fluoronitrobenzene → 2-[2-(4-Nitroanilino)ethyl]pyridine
https://huagongshe.com/reaction/33088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Pyridineethanamine | HCID 75919 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-[2-(4-Nitroanilino)ethyl]pyridine | HCID 13301713 | 95.7% |
Reaction Steps
2 g of 4-fluoronitrobenzene, 2.07 g of 2-(2-aminoethyl)pyridine, and 2.35 g of K2CO3 were added to a solution of 20 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 18 hours and, after cooling to room temperature, was then poured into a water+ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 3.3 g of N-(4-nitrophenyl)-N-(2-pyrid-2-ylethyl)amine (5) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429278B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-47aeb07bfb9d4ffcbb19763c34e2f767 |
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| Source note | uspto-grants-2008_09 |
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