HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 4-azido-3-ethoxy-N-ethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-amino-3-ethoxy-N-ethylbenzamide | HCID 63358549 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4-azido-3-ethoxy-N-ethylbenzamide | HCID 86629805 | 85% |
Reaction Steps
To a solution of 4-amino-3-ethoxy-N-ethylbenzamide (0.53 g) obtained in Example 131c) in 0.2N hydrochloric acid (12.5 ml) was added 1M aqueous sodium nitrite solution (2.5 ml) under ice-cooling, and the mixture was stirred for 2 hr. To the obtained reaction mixture was added an aqueous solution (5 ml) of sodium azide (0.17 g) under ice-cooling, and the mixture was stirred for 30 min. The reaction mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a yellow oil (0.50 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803822B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-0c80758f338a4dcb9963d20409d2dab9 |
| Source note | uspto-grants-2010_09 |