Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1662941Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1662941

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanone, 1-(5-amino-2-nitrophenyl)-HCID 6420386—
EduktHydrobromide monohydrateHCID 22326455—
EduktSodium NitriteHCID 23668193—
Produkt1-(5-Bromo-2-nitrophenyl)ethanoneHCID 12224157—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

In the ice bath, the starting material, about 10 mmol of 3-acetyl-4-nitro-aminobenzene was added into HBr/H2O (about 100 mL, 1/2, v/v), and sodium nitrite solution was gradually added. The solution was stirred at about 60° C. for about 2 hours. After the reaction was completed, the precipitate was filtered. The filtered solution was neutralized with about 1N NaOH, and extracted with EtOAc. Then the extracted material was dried with sodium sulfate anhydride. Next, the dried material was distilled under reduced pressure. Then, 3-acetyl-4-nitro-bromobenzene was obtained in a form of about 75% yellow oil using silica gel column chromatography (Hexane/EtOAc=2/1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08034747B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-2584ff91657842e0ab26364f0533adf3
Quellennotizuspto-grants-2011_10