HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-nitrophenyl)pyrrolidin-2-one → 1-(3-Aminophenyl)pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-nitrophenyl)pyrrolidin-2-one | HCID 1512870 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Aminophenyl)pyrrolidin-2-one | HCID 683956 | 100% |
Reaction Steps
A suspension of 1-(3-nitrophenyl)pyrrolidin-2-one (3.0 g, 15 mmol) in ethanol (50 ml) was heated until complete solution was obtained. The solution was cooled to ambient temperature then treated with 10% palladium on charcoal (150 mg) and hydrogenated at 50 psi until hydrogen uptake ceased (ca. 2 hours). The mixture was filtered through a glass microfibre filter paper (Whatman GF/A) and evaporated to dryness to give 1-(3-aminophenyl)pyrrolidin-2-one as a pale green oil (2.6 g, 100%) which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723735B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-413d825ca72a4efc985dce8771bdc787 |
| Source note | uspto-grants-2004_04 |