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HRID 1720184作成日:2026年10月26日

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/1720184

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Methyl 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—
触媒Sodium MethoxideHCID 10942334—
溶媒TolueneHCID 1140—
生成物methyl 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—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05504078
出典データセットuspto-grants-1996_04
ORD IDord-d7546855f1c743ad85812499526df50f
出典メモuspto-grants-1996_04