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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050661Generated: November 2, 2026

3-O-Benzyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose → 3-O-Benzyl-1,2-O-isopropylidene-alpha-D-glucofuranose

https://huagongshe.com/reaction/2050661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-O-Benzyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranoseHCID 97907—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-O-Benzyl-1,2-O-isopropylidene-alpha-D-glucofuranoseHCID 1108818887%

Reaction Steps

Crude 3-O-benzyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose (6) (23.5 g, 75.6 mmol) was dissolved in a 1:1:1 mixture of methanol, acetic acid and water (200 ml) and stood at 50° C. for 16 hours. The solvents were evaporated and the crude syrup purified by flash chromatography (ethyl acetate-hexane 3:2) to give 3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose (18.1 g, 87%) as a clear oil, [α]20D -49.9° (c, 1.08 in chloroform) [lit.44 -50.8° (c, 1.24 in chloroform)]; 1H NMR δ 1.33, 1.49 (6H, 2×s, acetonide); 2.17 (2H, bs, 2×OH); 3.69, 3.81 (2H, 2×dd, H-6,6', J6,6' 11.4 Hz, J5,6 5.5 Hz, J5,6' 3.4 Hz); 4.00-4.15 (3H, m, H-3, H-4, H-5); 4.56, 4.73 (2H, 2×d, CH2Ph, JH,H' 11.7 Hz); 4.63 (1H, d, H-2); 5.94 (1H, d, 1-H,J1,2 3.7 Hz); 7.31-7.38 (5H, m, H-Ph).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013842
Source datasetuspto-grants-1991_05
ORD IDord-926aa6f1afec4d9c93b36861300c761d
Source noteuspto-grants-1991_05