HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-2-nitropyridin-3-ol | HCID 21873808 | — |
| Catalyst | Ethyl bromoacetate | HCID 7748 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate | HCID 59560649 | 89% |
Reaction Steps
2-Bromo-5-hydroxy-6-nitropyridine (30 g, 0.14 mole) was suspended in acetone (200 ml), and potassium carbonate (39 g, 0.28 mole) was added, followed by ethyl bromoacetate (15.7 ml, 0.14 mmole). The reaction was heated at reflux for 10 hr, then was cooled to room temperature and diluted with Et2O. The precipitate was removed by suction filtration, and the filtrate was concentrated in vacuo to afford material (38 g, 89%), which was used without further purification; MS (ES) m/z 305.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691850B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-d3e7e008c76d4b32a256040140b882b0 |
| Source note | uspto-grants-2010_04 |