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Boron trifluoride → 1-Naphthol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Boron trifluoride | HCID 6356 | — |
| 反応物 | 1-Naphthol | HCID 7005 | — |
| 反応物 | beta-D-Ribofuranose, 1-acetate 2,3,5-tribenzoate | HCID 81455 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-Naphthol | HCID 7005 | — |
| 生成物 | HCID 18731516 | HCID 18731516 | — |
反応手順
A solution 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose (500 mg, 0.99 mmol), α-naphthol (428 mg, 3.00 mmol) and boron trifluoride diethyletherate (141 mg, 0.99 mmol. 125 μl) in dry dichloromethane (5 ml) was stirred at room temperature under argon for 16 hours. The mixture was worked up as for Stage 1 of Example 1 and purified by flash chromatography on silica gel (eluting with dichloromethane:hexanes, 3:2) to afford the title compound contaminated with α-naphthol. The latter was removed by dissolving the residue in ethyl acetate and washing with 10% aqueous sodium hydroxide solution, which after conventional processing, gave 136 mg, 23% of product as a yellow gum.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06379911B2 |
| 出典データセット | uspto-grants-2002_04 |
| ORD ID | ord-d29c5ad3b72a470cbe102ea3c53a1c86 |
| 出典メモ | uspto-grants-2002_04 |