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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33086Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/33086

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-FluoronitrobenzeneHCID 9590—
EduktPotassium CarbonateHCID 11430—
Edukt2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amineHCID 2310483792,8%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429278B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-7a84c7f876da493c8419e1d65ad26d6e
Quellennotizuspto-grants-2008_09