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HRID 25469作成日:2026年10月25日

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

https://huagongshe.com/reaction/25469

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Diacetone-D-glucoseHCID 7067560—
反応物DMSO acetic anhydrideHCID 86609981—
生成物1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-allofuranoseHCID 7157054—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858726B2
出典データセットuspto-grants-2005_02
ORD IDord-a62ddce00f3040878d58f6747e85353c
出典メモuspto-grants-2005_02