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HRID 261902Erstellt: 26. Oktober 2026

N,N-Diethylaniline → 4-Chloro-3,5-dinitrotoluene

https://huagongshe.com/reaction/261902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DiethylanilineHCID 7061—
EduktCalcium CarbonateHCID 10112—
Edukt2,6-Dinitro-p-cresolHCID 11872—
EduktPhosphorus oxychlorideHCID 24813—
Produkt4-Chloro-3,5-dinitrotolueneHCID 78918—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

About 100 parts (0.43 mol) of 4-hydroxy-3,5-dinitrotoluene, about 750 parts by volume of phosphorus oxychloride and about 1250 parts by volume of diethylaniline which has been dried over calcium carbonate are heated together to about 90° C. for about 21/2 hours with stirring. The reaction mixture is poured onto ice and extracted with methylene chloride, and the methylene chloride is removed in a rotary evaporator. After recrystallization from ethanol, about 65 parts of 4-chloro-3,5-dinitrotoluene of melting point of about 112° C. to about 113° C. about 70% of the theoretical yield is obtained. About 52 parts (0.24 mol) of this isolated compound are dissolved in about 500 parts by volume of toluene and added dropwise to a boiling mixture of about 180 parts of deoiled iron into about 180 parts by volume of H2O, about 280 parts by volume of toluene and about 5 parts by volume of glacial acetic acid. After about 3 hours, the reaction mixture is removed from the iron by suction filtration and then extracted with boiling toluene. The water is removed in a separating funnel and the organic phase is removed under vacuum. About 34 parts (91% of theoretical) of 4-chloro-3,5-diaminotoluene, melting point about 116° C. are obtained as white needles from 1:1 benzene/cyclohexane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152510
Quelldatensatzuspto-grants-1979_05
ORD IDord-cc08456cdf104a979bc0b1b35080a898
Quellennotizuspto-grants-1979_05