HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 2-Ethoxy-4-nitro-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-4-nitrobenzonitrile | HCID 286148 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Ethoxy-4-nitro-benzonitrile | HCID 21483723 | — |
Reaction Steps
To a solution of 2-hydroxy-4-nitrobenzonitrile (0.5 g, 3.04 mmol) in DMF (5 ml) is added-potassium carbonate (0.631 g, 4.56 mmol) followed by bromoethane (0.238 ml, 3.19 mmol) and the reaction mixture is stirred at room temperature for 5 days. The solvent is removed in vacuo and the crude is partitioned between ethyl acetate (100 ml) and water (100 ml). The organic layer is separated, washed with water (2×100 ml), saturated sodium hydrogen carbonate solution (100 ml) and concentrated in vacuo to afford the titled compound as a pale yellow solid which is used crude in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169251B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-5f83e34358eb42b3b22713721ab5ea50 |
| Source note | uspto-grants-2015_10 |