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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25469생성일: 2026년 10월 23일

Acetic Anhydride → 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-allofuranose

https://huagongshe.com/ko/reaction/25469

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Diacetone-D-glucoseHCID 7067560—
반응물DMSO acetic anhydrideHCID 86609981—
생성물1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-allofuranoseHCID 7157054—

반응 단계

Sowa, W. and Thomas, G. H. S., (Can. J. of Chem., 1966, Vol. 44, 836-838) used the DMSO/acetic anhydride oxidation of 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose in small scale (10 mmole) using a 20 fold excess of acetic anhydride. The ulose was then reduced providing 1,2:5,6-di-O-isopropylidene-α-D-allofuranose of poor quality, thus the product had to be column purified. Overall this procedure is not suitable for large-scale productions due to the large reagent consumption, two step procedure and the column purification step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858726B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a62ddce00f3040878d58f6747e85353c
출처 메모uspto-grants-2005_02