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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720182Generated: October 30, 2026

Methanol → methyl 2,3,4-tri-O-benzyl-6-O-(2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-alpha-D-glucopyranoside

https://huagongshe.com/reaction/1720182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 53849711—
CatalystSodium MethoxideHCID 10942334—
SolventTolueneHCID 1140—
Productmethyl 2,3,4-tri-O-benzyl-6-O-(2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-alpha-D-glucopyranosideHCID 53688273—

Reaction Steps

Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside (2.314 g, 2.46 mmol) is dissolved in hot toluene (20 ml) and methanol (80 ml) is added, followed by a few drops of 1 M methanolic sodium methoxide. The mixture is stirred at room temperature during 2 h. The reaction mixture is made neutral with Amberlite IR 120 (H+) resin, filtered and concentrated under reduced pressure so as to afford methyl 2,3,4-tri-O-benzyl-6-O-(2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-α-D -glucopyranoside as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504078
Source datasetuspto-grants-1996_04
ORD IDord-8a34d3b7ddd64f178c576328bb59f923
Source noteuspto-grants-1996_04