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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962657Generated: October 26, 2026

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

https://huagongshe.com/reaction/962657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DibromoanilineHCID 12004—
ReactantSodium NitriteHCID 23668193—
ReactantTin chloride monohydrateHCID 45051637—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product(2,4-Dibromophenyl)hydrazine hydrochlorideHCID 1649535075.9%

Reaction Conditions

Temperature5 °C

Reaction Steps

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 50° 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##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760051
Source datasetuspto-grants-1998_06
ORD IDord-bb483c19e4d14d34a12272cf926554bc
Source noteuspto-grants-1998_06