HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-Fluorobenzoyl)-3-hydroxypyridine | HCID 22987978 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate | HCID 10881213 | 102.1% |
Reaction Steps
A mixture of give 2-(4-fluorobenzoyl)-3-hydroxypyridine (2.2 g, 11.3 mmol), ethyl bromoacetate (1.6 ml, 14.15 mmol) and potassium carbonate (4.34 g, 31.4 mmol) in acetone (40 ml) was heated at reflux. After 3 h, the reaction was cooled to room temperature, filtered and concentrated in vacuo to give ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate (3.5 g) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316464B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-cda20e115c294458aca40971cfc00fe4 |
| Source note | uspto-grants-2001_11 |