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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64248Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktTri-O-benzyl-D-glucalHCID 11742644—
EduktPropan-2-one--dichloromethane (1/1)HCID 21584124—
EduktPotassium hydroxy sulfiteHCID 23707502—
LösungsmittelWaterHCID 962—
Produktallyl 3,4,6-tri-O-benzyl-beta-D-glucopyranosideHCID 1102737750%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447133B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-bba88a93227143cebe8f3aba0f22b6a6
Quellennotizuspto-grants-2016_09