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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466905Erstellt: 24. Oktober 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/de/reaction/466905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TrimethylpyridineHCID 7953—
EduktMethyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 11190476—
Edukt4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl chlorideHCID 54403365—
KatalysatorSilver perchlorateHCID 24562—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 53849711—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05157116
Quelldatensatzuspto-grants-1992_10
ORD IDord-ea2e577b99044a9fbcce7033137ab7e9
Quellennotizuspto-grants-1992_10