HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(4-Aminophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | 2-(4-Aminophenyl)acetamide | HCID 238034 | — |
Reaction Steps
To a suspension of Nitrobenzene (NB-2-A13, NB-2-A14 or NB-3-A16; 1.61 mmol) and Raney Ni (50 mg) in refluxing ethanol (10 mL) was added drop-wise anhydrous hydrazine (0.5 mL). After the addition was complete, the mixture was refluxed for an additional 20 minutes and then filtered through a pad of Celite. The Celite bed was washed with ethanol (100 mL) and the combined solution was evaporated under reduced pressure to provide pure 2-(4-aminophenyl)-acetamide (2-NB-2-A13, 2-NB-2-A14 or 2-NB-3-A16).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07692005B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-bf03270b059c4d4cbdbf83f0b49e3002 |
| Source note | uspto-grants-2010_04 |