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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45664Erstellt: 23. Oktober 2026

p-Nitroacetophenone → p-Aminoacetophenone

https://huagongshe.com/de/reaction/45664

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-NitroacetophenoneHCID 7487—
EduktAmmonium ChlorideHCID 25517—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produktp-AminoacetophenoneHCID 746863,1%

Reaktionsschritte

Into a 100-mL 3-necked round-bottom flask, was placed a solution of 1-(4-nitrophenyl)ethanone (6 g, 36.36 mmol, 1.00 equiv) in ethanol (100 mL), water (15 mL). This was followed by the addition of NH4Cl (3.85 g, 72.64 mmol, 2.00 equiv) in several batches. To this was added Fe (10.18 g, 181.79 mmol, 5.00 equiv) in several batches, while the temperature was maintained at reflux. The resulting mixture was heated to reflux for 2 h. The solids were filtered out and the resulting filtrate was concentrated under vacuum. The residue was diluted with 50 mL of water. The resulting solution was extracted with 3×50 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 3.1 g (60%) of 1-(4-aminophenyl)ethanone as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541448B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-07dedcf575804d12ae737fff1c6788ab
Quellennotizuspto-grants-2013_09