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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693333Generated: October 29, 2026

Acetic Anhydride → HCID 59311490, compound

https://huagongshe.com/reaction/1693333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Ethyl-2,3,5-trimethyl-1-oxo-1lambda~5~-pyridineHCID 67279988—
ProductHCID 59311490HCID 5931149076%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158638B2
Source datasetuspto-grants-2012_04
ORD IDord-196edf87bcb145518cbf6988aff65fb9
Source noteuspto-grants-2012_04