HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-Ethoxy-3-nitropyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloro-3-nitropyridin-2-ylamine | HCID 2724035 | — |
| Product | 6-Ethoxy-3-nitropyridin-2-amine | HCID 13245771 | — |
Reaction Steps
2.4 g of 60% sodium hydride was slowly added to 100 ml of ethanol and stirred as it was at room temperature for 10 minutes. 10 g of 2-amino-6-chloro-3-nitropyridine was added thereto and reacted at room temperature for 30 minutes. After concentration, water was added thereto, and it was extracted with ethyl acetate. It was washed with water and brine sucsessively, and dried over anhydrous sodium sulfate. After concentration, 9.7 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583138B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-cb8a7275956a4321b4f8d8517092a4ce |
| Source note | uspto-grants-2003_06 |