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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223522Generated: October 26, 2026

Acetic Anhydride → 3,5-Dioxohexanoic acid

https://huagongshe.com/reaction/223522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-Formyl-3-hydroxy-4,5-dihydroxymethylpyridine hydrochlorideHCID 88706593—
SolventTetrahydrofuranHCID 8028—
Product3,5-Dioxohexanoic acidHCID 5459844—

Reaction Steps

A solution of one equivalent of 2-formyl-3-hydroxy-4,5-dihydroxymethylpyridine hydrochloride in 400 ml. anhydrous tetrahydrofuran is treated with four equivalents of triethylamine and aged for one hour at room temperature. Then three equivalents of acetic anhydride are introduced, and the reaction mixture is aged 4 hours at room temperature. The reaction mixture is concentrated under reduced pressure to a gum. This is treated with a mixture of 300 ml. of diethyl ether and 300 ml. of distilled water. After shaking well, the layers are separated and the ether layer is dried over magnesium sulfate. After evaporation to dryness, the desired triacetate is obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355034
Source datasetuspto-grants-1982_10
ORD IDord-379862411fe243c993bcfb596c0d74af
Source noteuspto-grants-1982_10