HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 3-ethoxy-N-ethyl-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-ethyl-3-hydroxy-4-nitrobenzamide | HCID 21029708 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-ethoxy-N-ethyl-4-nitrobenzamide | HCID 68515126 | 30% |
Reaction Steps
To a solution of N-ethyl-3-hydroxy-4-nitrobenzamide (2.10 g) obtained in Example 131a) in acetone (100 ml) were added ethyl bromide (0.75 ml) and potassium carbonate (1.38 g), and the reaction mixture was heated under reflux overnight. The reaction mixture was allowed to cool to room temperature and the solvent was evaporated under reduced pressure. Ethyl acetate and water were added to the residue. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a pale-brown solid (0.72 g, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803822B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-9ead7259b1fd45b5bfccfd41b0cf1cd1 |
| Source note | uspto-grants-2010_09 |