HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357182Generated: November 1, 2026
Hydrochloric Acid → 4-acetyloxy-6-(benzyloxy)methyl-3,5-dimethyl-2H-pyran-2-one
https://huagongshe.com/reaction/1357182
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methyl 6-benzyloxy-2,4-dimethyl-3,5-dioxohexanoate | HCID 12082881 | — |
| Product | 4-acetyloxy-6-(benzyloxy)methyl-3,5-dimethyl-2H-pyran-2-one | HCID 12082882 | — |
Reaction Steps
An aqueous solution (6 ml) of LiOH-hydrate (64 mg) was added to a solution of methyl 6-benzyloxy-2,4-dimethyl-3,5-dioxohexanoate (430 mg) in THF (10 ml), and the mixture was stirred at room temperature for 1.5 hours. The reaction solution was neutralized with diluted hydrochloric acid, and after distilling off the volatile components under reduced pressure, extraction was performed with AcOEt at pH 3. The organic layer was dried with MgSO4 and then filtered and concentrated. Ac2O (6 ml) was added to the residue, and after stirring at room temperature for 30 minutes, pyridine (4 ml) was added and the mixture was stirred at room temperature for one hour. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/AcOEt=3/1→12/5) to obtain 4-acetyloxy-6-(benzyloxy)methyl-3,5-dimethyl-2H-pyran-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06589984B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-73518805d6fa40d2bd124df88032c3f1 |
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| Source note | uspto-grants-2003_07 |
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