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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466908Generated: October 27, 2026

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

https://huagongshe.com/reaction/466908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethy-alpha-D-glucopyranosyl)-2,3,6-tri-O-benzyl-alpha-D-glucopyranosideHCID 54010971—
SolventTolueneHCID 1140—
Productmethyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-hydroxymethyl-alpha-D-glucopyranosyl)-2,3,6-tri-O-benzyl-alpha-D-glucopyranosideHCID 53787003—

Reaction Steps

Methyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethy-α-D-glucopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside (3.19 g, 3.35 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 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-hydroxymethyl-α-D-glucopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157116
Source datasetuspto-grants-1992_10
ORD IDord-99369ba750c54c1892470b47280e79a8
Source noteuspto-grants-1992_10