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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747341Generated: October 27, 2026

Acetic Acid → 2-Acetoxymethyl-3-methyl-pyridine

https://huagongshe.com/reaction/747341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
Reactant2,3-LutidineHCID 11420—
SolventAcetic AnhydrideHCID 7918—
Product2-Acetoxymethyl-3-methyl-pyridineHCID 10749557—

Reaction Steps

To a stirred solution of 2,3-lutidine (4.8363 g, 45.13 mmol) in glacial acetic acid (30 mL) at room temperature was added 30% H2O2 (4.6 mL) and the resultant solution was heated to 70° C. After 6 hours, the reaction mixture was cooled to room temperature, additional H2O2 (4.6 mL) was added, and the solution was heated at 70° C. overnight. The reaction mixture was allowed to cool to room temperature and then concentrated under reduced pressure. The residue was dissolved in CHCl3 (100 mL) and treated with solid Na2CO3 (14.12 g). After 1 hour, the supernatant was decanted and the residue was washed with warm CHCl3 (3×50 mL). The combined supernatants were filtered and concentrated to provide 4.6951 g as a yellow solid. The solid was dissolved in acetic anhydride (38 mL) and heated at 90° C. overnight. The mixture was cooled to room temperature and concentrated and the crude product was filtered through a silica plug (33 g silica, ethyl acetate) to give 6.13 g of 2-acetoxymethyl-3-methyl-pyridine as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396840B2
Source datasetuspto-grants-2008_07
ORD IDord-866cfd8e0533452682d40516ac6e9f88
Source noteuspto-grants-2008_07