HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 3-(2-ethoxy-2-oxoethoxy)picolinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-hydroxypicolinate | HCID 15080989 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 3-(2-ethoxy-2-oxoethoxy)picolinate | HCID 21793317 | 82.2% |
Reaction Steps
A mixture of ethyl 3-hydroxy-picolinate (11.0 g, 65.8 mmol), ethyl bromoacetate (12.1 g, 72.4 mmol) and anhydrous potassium carbonate (11.8 g, 85.5 mmol) in acetone (120 mL) was heated under reflux for 15 h. After cooling, the inorganic material separated by filtration. The filtrate was dissolved in chloroform, washed with water, then brine and dried (MgSO4), filtered, and the solvent was evaporated to give a brown oily residue. The residue was purified by flash chromatography using a gradient of ammoniated methanol in chloroform to give ethyl 2-(2-ethoxycarbonyl-3-pyridyloxy)acetate (13.7 g) as a yellow oil (13.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544693B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-57c4a3b67f9b4d5b90b1641d493067d9 |
| Source note | uspto-grants-2009_06 |