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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64248Generated: October 26, 2026

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

https://huagongshe.com/reaction/64248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTri-O-benzyl-D-glucalHCID 11742644—
ReactantPropan-2-one--dichloromethane (1/1)HCID 21584124—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Productallyl 3,4,6-tri-O-benzyl-beta-D-glucopyranosideHCID 1102737750%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447133B2
Source datasetuspto-grants-2016_09
ORD IDord-bba88a93227143cebe8f3aba0f22b6a6
Source noteuspto-grants-2016_09