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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372159Generated: October 31, 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/2372159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
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—
SolventTolueneHCID 1140—
Productmethyl 2,3,4-tri-O-benzyl-6-O-(2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-alpha-D-glucopyranosideHCID 53688273100.1%

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) was dissolved in hot toluene (20 mL) and methanol (80 mL) was added, followed by a few drops of 1M. methanolic sodium methoxide. The mixture was stirred at room temperature during 2 h. The reaction mixture was made neutral with Amberlite IR 120 (H+) resin, filtered and concentrated under reduced pressure to afford methyl 2,3,4-tri-O-benzyl-6-O-(2,3,6-tri-O-benzyl-α-D-galactopyranosyl) -α-D-glucopyranoside (2.21 g, 100%) as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05097023
Source datasetuspto-grants-1992_03
ORD IDord-c157f87529b84f9eac8d59e326b6be76
Source noteuspto-grants-1992_03