HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-nitrocinnamate → Ethyl 3-(4-aminophenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-nitrocinnamate | HCID 1268038 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(4-aminophenyl)propanoate | HCID 10442595 | 95% |
Reaction Steps
(E)-Ethyl 3-(4-nitrophenyl)acrylate (11.7 g, 52.9 mmol) in tetrahydrofuran (100 ml) was hydrogenated over 10% Palladium-Carbon (1.20 g) at atmospheric pressure. After removal of the catalyst, the filtrate was concentrated in vacuo to give ethyl 3-(4-aminophenyl)propionate as a yellow oil (9.66 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235731B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-bef6075fa2cb49bc864e5e9b58ccb849 |
| Source note | uspto-grants-2001_05 |