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HRID 466905作成日:2026年10月27日

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/466905

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Methyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 11190476—
反応物4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl chlorideHCID 54403365—
触媒Silver perchlorateHCID 24562—
溶媒Diethyl EtherHCID 3283—
生成物Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 53849711—

反応条件

温度-30 °C

反応手順

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.

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-ea2e577b99044a9fbcce7033137ab7e9
出典メモuspto-grants-1992_10