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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542913생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/542913

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물PyridineHCID 1049—
반응물Antimony pentachlorideHCID 24294—
반응물aldehydo-D-XyloseHCID 644160—
생성물alpha-D-Xylofuranose, 1,2:3,5-bis-O-(1-methylethylidene)-HCID 3033789.2%

반응 조건

온도60 °C

반응 단계

To 200 ml of acetone were added 10.0 g of D-xylose and 89.7 mg of antimony pentachloride, and the mixture was refluxed with stirring in a water bath of 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 condenser. After completion of the reaction, a small amount of pyridine was added to the reaction solution, 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 solution and water successively, and dried over anhydrous magnesium sulfate. The benzene was distilled off under reduced pressure, and the resulting residue was distilled under reduced pressure to give 13.7 g (89.2%) of 1,2:3,5-di-O-isopropylidene-α-D-xylofuranose as a fraction of 94 to 97° C./3 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04659809
출처 데이터셋uspto-grants-1987_04
ORD IDord-cdda35667050407b8c5d36a26ed1a9d9
출처 메모uspto-grants-1987_04