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HRID 374402作成日:2026年10月25日

Ethanol → 2-Acrylamido-2-deoxy-D-glucose

https://huagongshe.com/reaction/374402

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Acryloyl chlorideHCID 13140—
反応物(3R,4R,5S,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol hydrochlorideHCID 2723635—
反応物Sodium NitriteHCID 23668193—
溶媒Potassium CarbonateHCID 11430—
生成物2-Acrylamido-2-deoxy-D-glucoseHCID 22858156—

反応条件

温度0 °C

反応手順

Glucosamine hydrochloride (0.1 mol; 21.56 g) and sodium nitrite (0.2 g) as inhibitor were dissolved under nitrogen atmosphere in 100 ml of a 0.3 M potassium carbonate solution, and the mixture was cooled to 0° C. Under vigorous stirring, acryloyl chloride (0.2 mol; 18.1 g) was added while the temperature was kept below 5° C. Stirring was continued for 3 h at 0°-5° C. and further 2 h while the mixture was allowed to come to room temperature. Finally, it was left at room temperature for 14 h. The solution was poured into 1 l of dry ethanol and strongly mixed. The resulting suspension was filtered by suction, and the cake was washed three times with 250 ml of 95% ethanol. To the combined filtrates and washings 1 l of ether was added and the solution was kept at 0° C. for 24 h. The desired product crystallized as white cubes, while the yellowish needles that might appear were a by-product. It could be separated by stirring up the whole mixture and decanting the liquid with the floating needles while the product remained on the ground of the reaction flask. By addition of 1 l of ether to the mother liquid a second crop could be isolated. The product was recrystallized two times from water/ethanol/ether. Yield 8.1-10.5 g (35-45%), m.p.:124°-125° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05480790
出典データセットuspto-grants-1996_01
ORD IDord-25d9e7780cf346639ca19a894be80314
出典メモuspto-grants-1996_01