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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1462578생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1462578

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Hydrochloric AcidHCID 313—
반응물1,4-DioxaneHCID 31275—
반응물Sodium BicarbonateHCID 516892—
반응물aldehydo-D-XyloseHCID 644160—
생성물alpha-D-Xylofuranose, 1,2:3,5-bis-O-(1-methylethylidene)-HCID 3033783.7%

반응 조건

온도60 °C

반응 단계

To 200 ml of acetone were added 10.0 g of D-xylose, 138 mg of cupric fluoride dihydrate and 1 ml of a 2 mole/l solution of hydrogen chloride in dioxane, and the mixture was stirred for 7 hours under reflux on a warm-water bath at 60° C. The refluxing solvent was continuously dried with 20 g of molecular sieves 3A (produced by Wako Pure Chemical Ind., Ltd.) which was placed between the reaction vessel and the cooling tube. After the conclusion of the reaction, a small amount of aqueous sodium hydrogencarbonate was added to the reaction mixture and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene, and the solution was washed with aqueous sodium hydrogencarbonate and water, and dried over anhydrous magnesium sulfate. When the benzene was distilled off under reduced pressure, there was obtained 12.8 g (83.7%) of 1,2:3,5-di-O-isopropylidene-α-D-xylofuranose as a residue in the form of an oily material (purity of not less than 97%). The compound showed a boiling point of 94° to 97° C./3 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04460767
출처 데이터셋uspto-grants-1984_07
ORD IDord-d7124bfea8e944dcb477d7c30b695e1c
출처 메모uspto-grants-1984_07