Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343435Erstellt: 25. Oktober 2026

2,4-Dibromoaniline → (2,4-Dibromophenyl)hydrazine hydrochloride

https://huagongshe.com/reaction/343435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-DibromoanilineHCID 12004—
EduktSodium NitriteHCID 23668193—
EduktTin chloride monohydrateHCID 45051637—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Produkt(2,4-Dibromophenyl)hydrazine hydrochlorideHCID 1649535075,9%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a stirred, cooled (-5° C.) solution of 2,4-dibromoaniline (50.0 g,0.2 mol.) in concentrated HCl solution (110 mL) was added sodium nitrite (13.8 g, 0.2 mol.) in water (110 mL) dropwise at such a rate as to maintain temperature below 5° C. After complete addition, the mixture was further stirred at 5° C. for 30 minutes. A solution of tin chloride monohydrate (135.4 g, 0.6 mol.) in concentrated HCl (total volume 170 mL) was added dropwise again maintaining temperature below 5° C. After complete addition and 30 minutes of further stirring, the mixture was placed in the freezer overnight. The light brown solid which precipitated was isolated by filtration and washed with cold brine followed by a solution of petroleum ether/diethyl ether (2/1 by volume). This solid was slowly added to an ice cooled mixture of 50% sodium hydroxide solution/ethyl acetate. The mixture was extracted with ethyl acetate and the organic phase dried over magnesium sulfate. After filtration, the solution was concentrated to 400 mL total volume , diluted with diethyl ether (1.5 L) and treated with dry HCl. The product, 2,4-dibromophenyl-hydrazine hydrochloride (45.9 g) was isolated as a white solid and used without further purification. ##STR24##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861425
Quelldatensatzuspto-grants-1999_01
ORD IDord-1c90f00fe3214060862d7d2f3753ee4f
Quellennotizuspto-grants-1999_01