HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45664Generated: October 25, 2026
p-Nitroacetophenone → p-Aminoacetophenone
https://huagongshe.com/reaction/45664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-Aminoacetophenone | HCID 7468 | 63.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541448B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-07dedcf575804d12ae737fff1c6788ab |
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| Source note | uspto-grants-2013_09 |
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