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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33086Generated: October 26, 2026

p-Fluoronitrobenzene → N-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amine

https://huagongshe.com/reaction/33086

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amineHCID 2310483792.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

2 g of 4-fluoronitrobenzene, 2.07 g of 2-(3-pyridyl)ethylamine, 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 16 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. 3.2 g of N-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amine (3) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429278B2
Source datasetuspto-grants-2008_09
ORD IDord-7a84c7f876da493c8419e1d65ad26d6e
Source noteuspto-grants-2008_09