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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720181Generated: October 26, 2026

2,4,6-Trimethylpyridine → Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranoside

https://huagongshe.com/reaction/1720181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantMethyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 11190476—
Reactant4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl chlorideHCID 54403365—
CatalystSilver perchlorateHCID 24562—
SolventDiethyl EtherHCID 3283—
ProductMethyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 53849711—

Reaction Conditions

Temperature-30 °C

Reaction Steps

Ethereal silver perchlorate (0.08 M, 76.9 ml, 6.15 mmol) is added With stirring at -30° C. to a solution of methyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside (2.078 g, 4.48 mmol), 4-O-acetyl-2,3,6-tri-O-benzyl-α-D-galactopyranosyl chloride (2,859 g, 5.6 mmol) and 2,4,6-trimethylpyridine (0.81 ml, 6.15 mmol) in ether (20 ml). The mixture is stirred 15 min at -30° C. and silver chloride precipitated. The mixture is filtered through a celite pad, the solids are washed with ether, the filtrate is concentrated under reduced pressure. The residue is dissolved in methylene chloride and the organic layer is washed successively with aqueous sodium thiosulfate and water. The organic layer is dried over sodium sulfate, filtered and concentrated under reduced pressure so as to afford a foam. Flash chromatography on silica gel and elution with a graded mixture of hexane and ethyl acetate will afford methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504078
Source datasetuspto-grants-1996_04
ORD IDord-e19a8d5b70bf47cbb25726cbb632299b
Source noteuspto-grants-1996_04