HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 59311490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Ethyl-2,3,5-trimethyl-1-oxo-1lambda~5~-pyridine | HCID 67279988 | — |
| Product | HCID 59311490 | HCID 59311490 | 76% |
Reaction Steps
A mixture composed of the above 4-ethyl-2,3,5-trimethylpyridine 1-oxide (3.84 g) and acetic anhydride (50 mL) was heated under reflux for 30 minutes. After leaving to cool to room temperature, the reaction solution was concentrated under reduced pressure. The residue was dissolved in chloroform and then washed with a saturated sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate-hexane) to obtain the title compound (3.64 g, 76%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158638B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-196edf87bcb145518cbf6988aff65fb9 |
| Source note | uspto-grants-2012_04 |