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HRID 230874作成日:2026年10月26日

beta-D-Galactose pentaacetate → 4-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuran

https://huagongshe.com/reaction/230874

反応式

関与物質

役割名称HCID仕込み量
反応物beta-D-Galactose pentaacetateHCID 94752—
反応物4-Hydroxy-3-(2-phenylethyl)benzofuranHCID 23103521—
溶媒DichloromethaneHCID 6344—
生成物4-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuranHCID 6713601549.5%

反応手順

To a solution of 4-hydroxy-3-(2-phenylethyl)benzofuran (0.11 g) and 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranose (0.37 g) in dichloromethane (5 mL) was added boron trifluoride-diethyl ether complex (0.12 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=3/1-3/2) to give 4-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuran (0.13 g). This material was dissolved in methanol (5 mL). To the solution was added sodium methoxide (28% methanol solution, 0.043 mL), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give the title compound (24 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566699B2
出典データセットuspto-grants-2009_07
ORD IDord-4c87c0f7e25f476eb12123bf1df46b81
出典メモuspto-grants-2009_07