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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703165Generated: October 30, 2026

Acetic Anhydride → 2-(Acetoxymethyl)-4-methoxy-3,5-dimethylpyridine

https://huagongshe.com/reaction/703165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Methoxy-2,3,5-trimethylpyridine 1-oxideHCID 10702237—
SolventChloroformHCID 6212—
Product2-(Acetoxymethyl)-4-methoxy-3,5-dimethylpyridineHCID 5067289—

Reaction Steps

215 ml of acetic anhydride were added dropwise at room temperature to a solution of 81.5 g of 4-methoxy-2,3,5-trimethylpyridine 1-oxide in 290 ml of chloroform. After boiling under reflux for 4 hours the solution was evaporated, the residue was dissolved in 200 ml of toluene and again evaporated. The residue was taken up in 500 ml of ethyl acetate and extracted three times with 250 ml of saturated sodium bicarbonate solution. The organic phase was dried over sodium sulfate and evaporated in vacuo. The product which remains behind as the residue was chromatographed on 400 g of silica gel with ether. There was obtained (4-methoxy-3,5-dimethyl-2-pyridyl)methyl acetate in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04981861
Source datasetuspto-grants-1991_01
ORD IDord-34f23209505142ef8984cfcd38f9c469
Source noteuspto-grants-1991_01