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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45664Generated: October 25, 2026

p-Nitroacetophenone → p-Aminoacetophenone

https://huagongshe.com/reaction/45664

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-NitroacetophenoneHCID 7487—
ReactantAmmonium ChlorideHCID 25517—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productp-AminoacetophenoneHCID 746863.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541448B2
Source datasetuspto-grants-2013_09
ORD IDord-07dedcf575804d12ae737fff1c6788ab
Source noteuspto-grants-2013_09