Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230708Erstellt: 24. Oktober 2026

Ethanone, 1-(5-amino-2-nitrophenyl)- → 1-(5-Bromo-2-nitrophenyl)ethanone

https://huagongshe.com/de/reaction/230708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanone, 1-(5-amino-2-nitrophenyl)-HCID 6420386—
EduktHydrobromide monohydrateHCID 22326455—
EduktSodium NitriteHCID 23668193—
Produkt1-(5-Bromo-2-nitrophenyl)ethanoneHCID 1222415775%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

10 mmol of 3-acetyl-4-nitro-aminobenzene as a starting material was added to 100 mL of HBr/H2O (1/2, v/v) and a sodium nitrite solution was slowly added dropwise thereto in an ice bath. The reaction mixture was stirred at 60° C. for 2 hours. When the reaction was completed, the precipitate was filtered off. The filtrate was neutralized with 1N NaOH, extracted with EtOAc, dried over anhydrous sodium sulfate, distilled under reduced pressure and purified by silica gel column chromatography (hexane/EtOAc=2/1) to obtain the desired 3-acetyl-4-nitro-bromobenzene as a yellow oil (75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566773B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-0a65bf957c504fd4a9138c474b2d88c4
Quellennotizuspto-grants-2009_07