HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Ethoxy-5-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 2-Ethoxy-5-nitropyridine | HCID 295864 | — |
Reaction Steps
2-Chloro-5-nitropyridine was added to a homogeneous solution of potassium hydroxide (3.93 g, 70 mmol) in ethanol (35 mL) at ambient temperature. The reaction mixture was stirred for 1 h, then diluted with saturated aqueous ammonium chloride and cooled in an ice bath. The precipitate was collected, rinsed with water and dried to give 3.60 g of 2-ethoxy-5-nitropyridine as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399604B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-5a7bae2945164047815e982c3c85ea2e |
| Source note | uspto-grants-2002_06 |