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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 6-benzyloxy-2,4-dimethyl-3,5-dioxohexanoateHCID 12082881—
Product4-acetyloxy-6-(benzyloxy)methyl-3,5-dimethyl-2H-pyran-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589984B1
Source datasetuspto-grants-2003_07
ORD IDord-73518805d6fa40d2bd124df88032c3f1
Source noteuspto-grants-2003_07