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HRID 358126作成日:2026年10月26日

Acetone → alpha-D-Xylofuranose, 1,2:3,5-bis-O-(1-methylethylidene)-

https://huagongshe.com/reaction/358126

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物PyridineHCID 1049—
反応物Hydrogen iodideHCID 24841—
反応物aldehydo-D-XyloseHCID 644160—
生成物alpha-D-Xylofuranose, 1,2:3,5-bis-O-(1-methylethylidene)-HCID 3033783.6%

反応条件

温度60 °C

反応手順

To 200 ml of acetone were added 10.0 g of D-xylose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 60° C. for 5 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the cooling jacket. After completion of the reaction, a small amount of pyridine was added and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene and the benzene solution was washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The benzene was distilled off under reduced pressure and the residue was further distilled under reduced pressure, whereby 12.8 g (83.6%) of 1,2:3,5-di-O-isopropylidene-α-D-xylofuranose was obtained as a fraction boiling at 94°-97° C./3 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04464530
出典データセットuspto-grants-1984_08
ORD IDord-76a5f66a51094a61bd512b882d9b312c
出典メモuspto-grants-1984_08