HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(4-nitrophenyl)propionate → Ethyl 2-(4-aminophenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(4-nitrophenyl)propionate | HCID 3016550 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-aminophenyl)propanoate | HCID 118009 | — |
Reaction Steps
To a stirred solution of 2-(4-Nitro-phenyl)-propionic acid ethyl ester (3.67 g) in THF (40 mL) and EtOH (40 mL) was slowly added 10% Pd/C (405 mg) at room temperature. After hydrogenated for 20 h with H2 balloon, the reaction mixture was filtered through celite pad and washed with EtOAc. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The resulting residue was chromatographed on silica gel (n-Hex:EtOAc=4:1) to afford the product as pale yellow oil. (99.7%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785474B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-7880488443b14ce4ba52cb9a2ac81d39 |
| Source note | uspto-grants-2014_07 |