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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64248생성일: 2026년 10월 24일

Sodium Bicarbonate → allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranoside

https://huagongshe.com/ko/reaction/64248

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Tri-O-benzyl-D-glucalHCID 11742644—
반응물Propan-2-one--dichloromethane (1/1)HCID 21584124—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매WaterHCID 962—
생성물allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranosideHCID 1102737750%

반응 단계

3,4,6-tri-O-benzyl-D-glucal (7.2 g, 17.3 mmol) in CH2Cl2/acetone (2:1, 105 mL) and a saturated solution of NaHCO3 (100 mL) was added. The mixture was stirred vigorously while a solution of Oxone (21.2 g, 34.6 mmol) in water (150 mL) was added dropwise over 30 minutes. After 1.5 hours of vigorous stirring the layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×150 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated. The residue was co-evaporated with toluene (3×10 mL), dissolved in allyl alcohol (25 mL) and stirred at room temperature overnight. The reaction mixture was purified on a silica gel column (80 g) using an ISCO automated chromatography system, eluting with a 0→60% gradient of ethyl acetate in heptane, to give allyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside (4.2 g, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447133B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-bba88a93227143cebe8f3aba0f22b6a6
출처 메모uspto-grants-2016_09