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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 456857Erstellt: 24. Oktober 2026

N-Phenyl-p-phenylenediamine → N-[2-(4-nitrophenyl)-ethyl]-N'-[4-(phenylamino)phenyl]-urea

https://huagongshe.com/de/reaction/456857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Phenyl-p-phenylenediamineHCID 7564—
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
EduktBenzeneethanamine, 4-nitro-, hydrochloride (1:1)HCID 458983—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[2-(4-nitrophenyl)-ethyl]-N'-[4-(phenylamino)phenyl]-ureaHCID 2264637640%

Reaktionsschritte

0.5 g (1.7 mmol) of triphosgene is dissolved in 8 ml of dichloromethane in a 100 ml flask, under argon. Using a motorized syringe, a solution of 0.92 g (5 mmol) of 4-aminodiphenylamine and 1.44 ml (8.2 mmol) of diisopropylethylamine in 15 ml of dichloromethane is added over one hour. Five minutes after the addition is finished, 1.01 g (5 mmol) of 4-nitrophenethylamine hydrochloride followed by a solution of 1.44 ml (8.2 mmol) of diisopropylethylamine in 10 ml of dichloromethane are added in a single portion. After agitation for two hours at 20° C., the reaction mixture is diluted with 50 ml of dichloromethane and 20 ml of water. The organic phase is decanted and rewashed with 20 ml of water. After drying over, MgSO4 and filtration, the organic solution is partially concentrated under vacuum. The precipitate formed is collected by filtration and rinsed with dichloromethane. A yellow solid is obtained with a yield of 40%. Melting point: 204–205° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07186752B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-241df8e502d2419685b72757de2dc2fb
Quellennotizuspto-grants-2007_03