HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851966Generated: October 30, 2026
Ethanol → 2-Acetoxymethyl-5-methoxypyridine
https://huagongshe.com/reaction/851966
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Methoxy-2-methyl-1-oxo-1lambda~5~-pyridine | HCID 12214019 | — |
| Product | 2-Acetoxymethyl-5-methoxypyridine | HCID 14517152 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253158B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-0f495cf7a2294a069c2878e093280514 |
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| Source note | uspto-grants-2007_08 |
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