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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851966Generated: October 30, 2026

Ethanol → 2-Acetoxymethyl-5-methoxypyridine

https://huagongshe.com/reaction/851966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Methoxy-2-methyl-1-oxo-1lambda~5~-pyridineHCID 12214019—
Product2-Acetoxymethyl-5-methoxypyridineHCID 14517152—

Reaction Conditions

Temperature115 °C

Reaction Steps

5-Methoxy-2-methyl-pyridine 1-oxide (9.25 g, 66.5 mmol) was suspended in acetic anhydride (31 ml) under an argon atmosphere. The mixture was heated to ca.115° C. and this temperature was maintained for a further 5 h and the mixture turned black. Ethanol (2.5 ml) was added and the mixture was concentrated under reduced pressure. The residue was taken up in ethyl acetate and washed with 10% K2CO3 and water. The aqueous phases were back extracted with ethyl acetate and the combined organic phases were dried (MgSO4) filtered and concentrate under reduced pressure. The crude oil was purified using Kugelrohr distillation (90-100° C./0.1 mbar) yielding a colorless oil: 10.7 g (80%); 1H NMR (CDCl3) δ 2.13 (s, 3H), 3.86 (s, 3H), 5.16 (s, 2H), 7.18-7.31 (m, 2H), 8.30 (d, 1H) MS: m/e=181.2 (M), 138.0 (M−COCH3)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253158B2
Source datasetuspto-grants-2007_08
ORD IDord-0f495cf7a2294a069c2878e093280514
Source noteuspto-grants-2007_08