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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2119043생성일: 2026년 10월 26일

L-(-)-Sorbose → alpha-L-Sorbofuranose, 2,3:4,6-bis-o-(1-methylethylidene)-

https://huagongshe.com/reaction/2119043

반응식

참여 물질

역할이름HCID투입량
반응물L-(-)-SorboseHCID 6904—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Sodium BicarbonateHCID 516892—
용매AcetoneHCID 180—
생성물alpha-L-Sorbofuranose, 2,3:4,6-bis-o-(1-methylethylidene)-HCID 140270171%

반응 조건

온도-10 °C

반응 단계

A mixture of 20 g (111 millimoles) of L-sorbose, 200 μl (2.3 millimoles) of trifluoromethanesulfonic acid (TFMSA) and 400 ml of acetone (H2O content 0.1%) was refluxed for 4.5 hours. 40 g of a molecular sieve (3 Å) were present in a Soxhlet extractor between the reaction flask and the reflux condenser. When the reaction was complete, the reaction mixture was cooled to -10° C. and 10 ml of aqueous NaHCO3 solution were added. Thereafter, the acetone was distilled off under reduced pressure, the residue was taken up in 35 ml of H2O and the solution was extracted with 3 times 110 ml of toluene at 70° C. The combined toluene phases were washed with 7.5 ml of H2O and dried over Na2SO4, and the toluene was distilled off under reduced pressure to give 24.7 g (85.5%) of 2,3:4,6-di-O-isopropylidene-α-L-sorbofuranose (DAS). After the product had been recrystallized from toluene, its melting point was measured as 78°-79° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04681936
출처 데이터셋uspto-grants-1987_07
ORD IDord-b06980f1ee6246e2a47a81014d862e19
출처 메모uspto-grants-1987_07