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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461060Generated: October 26, 2026

Acetic Anhydride → 3,5-Dioxohexanoic acid

https://huagongshe.com/reaction/461060

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 numberUS04061759
Source datasetuspto-grants-1977_12
ORD IDord-c908c22ea75b4fa58dbc9dcf38690a96
Source noteuspto-grants-1977_12