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HRID 223522作成日:2026年10月25日

Acetic Anhydride → 3,5-Dioxohexanoic acid

https://huagongshe.com/reaction/223522

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物2-Formyl-3-hydroxy-4,5-dihydroxymethylpyridine hydrochlorideHCID 88706593—
溶媒TetrahydrofuranHCID 8028—
生成物3,5-Dioxohexanoic acidHCID 5459844—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04355034
出典データセットuspto-grants-1982_10
ORD IDord-379862411fe243c993bcfb596c0d74af
出典メモuspto-grants-1982_10