戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 466908作成日:2026年10月25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/466908

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium MethoxideHCID 10942334—
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—
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-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157116
出典データセットuspto-grants-1992_10
ORD IDord-99369ba750c54c1892470b47280e79a8
出典メモuspto-grants-1992_10