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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | beta-D-Galactose pentaacetate | HCID 94752 | — |
| 反応物 | 4-Hydroxy-3-(2-phenylethyl)benzofuran | HCID 23103521 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuran | HCID 67136015 | 49.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07566699B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-4c87c0f7e25f476eb12123bf1df46b81 |
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| 出典メモ | uspto-grants-2009_07 |
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