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HRID 1720184Erstellt: 24. Oktober 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/de/reaction/1720184

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktMethyl 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—
KatalysatorSodium MethoxideHCID 10942334—
LösungsmittelTolueneHCID 1140—
Produktmethyl 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—

Reaktionsschritte

Methyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethyl-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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05504078
Quelldatensatzuspto-grants-1996_04
ORD IDord-d7546855f1c743ad85812499526df50f
Quellennotizuspto-grants-1996_04