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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223522생성일: 2026년 10월 24일

Acetic Anhydride → 3,5-Dioxohexanoic acid

https://huagongshe.com/ko/reaction/223522

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물2-Formyl-3-hydroxy-4,5-dihydroxymethylpyridine hydrochlorideHCID 88706593—
용매TetrahydrofuranHCID 8028—
생성물3,5-Dioxohexanoic acidHCID 5459844—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04355034
출처 데이터셋uspto-grants-1982_10
ORD IDord-379862411fe243c993bcfb596c0d74af
출처 메모uspto-grants-1982_10