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HRID 1016226作成日:2026年10月27日

Benzyl Bromide → 2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl Fluoride

https://huagongshe.com/reaction/1016226

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物alpha-D-galactosyl fluorideHCID 10921145—
触媒Silver(II) oxideHCID 92152—
溶媒DimethylformamideHCID 6228—
生成物2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl FluorideHCID 9959029—

反応条件

温度-20 °C

反応手順

α-D-galactopyranosyl fluoride (2.30 g, 12.62 mmol) was dissolved in dry DMF (40 ml) and, at −20° C., benzyl bromide (12.95 g, 75.72 mmol) and silver oxide (10 g) were added. The reaction mixture was stirred at −20° C. for 5 h and then at room temperature for 24 h. The salts were then filtered off and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel (350 g) with 15:1 petroleum ether/ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06475486B1
出典データセットuspto-grants-2002_11
ORD IDord-cffac80fabff41b9adf82ecb8d529601
出典メモuspto-grants-2002_11