HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-ethoxy-N-ethyl-4-nitrobenzamide → 4-amino-3-ethoxy-N-ethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-ethoxy-N-ethyl-4-nitrobenzamide | HCID 68515126 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-amino-3-ethoxy-N-ethylbenzamide | HCID 63358549 | 84.2% |
Reaction Steps
To a solution of 3-ethoxy-N-ethyl-4-nitrobenzamide (0.72 g) obtained in Example 131b) in ethanol (15 ml) was added 10% Pd/C (50% wet) (0.07 g), and the mixture was stirred at room temperature overnight under a hydrogen atmosphere. The reaction mixture was filtered through celite, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column (ethyl acetate/hexane=1/1 to ethyl acetate) to give the title compound as a colorless oil (0.53 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803822B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-59560237a5f747348f8504953d8f599d |
| Source note | uspto-grants-2010_09 |