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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43325Erstellt: 24. Oktober 2026

Hydrogen Bromide → 4-Bromo-1-ethyl-2-nitrobenzene

https://huagongshe.com/de/reaction/43325

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
Edukt4-Ethyl-3-nitroanilineHCID 22708680—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
Produkt4-Bromo-1-ethyl-2-nitrobenzeneHCID 7566996—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

Hydrobromic acid (48% wt. in water, 240 ml) is added dropwise to a suspension of 4-ethyl-3-nitroaniline (20 g, 0.12 mol) in water (80 ml), and the mixture stirred until the solid is dissolved. The mixture is cooled to −5° C. and a solution of sodium nitrite (19.8 g, 0.28 mol) in water (100 ml) is added dropwise, maintaining the temperature at 0-5° C. Once the addition is complete, the cooling bath is removed and the reaction mixture is stirred for one hour at room temperature. The mixture is added dropwise to a pre-cooled solution of cuprous bromide (22.4 g, 0.16 mol) in hydrobromic acid (48% wt. in water) at 0° C. The reaction mixture is stirred and allowed to warm to room temperature over three hours. The mixture is extracted with diethyl ether, and the organic extracts are combined, dried over anhydrous sodium sulfate, filtered and the filtrate concentrated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with hexane to give 4-bromo-1-ethyl-2-nitrobenzene (18 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536351B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ccf2738d93d64552b45d91a18f557485
Quellennotizuspto-grants-2013_09