関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-(Chloromethyl)-4-Ethoxybenzene | HCID 2063971 | — |
| 反応物 | 1-(5-Hydroxy-1-benzofuran-2-yl)ethanone | HCID 3237877 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | 1-{5-[(4-Ethoxybenzyl)oxy]-1-benzofuran-2-yl}ethanone | HCID 67015866 | 163.5% |
反応手順
To a solution of 1-(5-hydroxy-1-benzofuran-2-yl)ethanone (2.40 g, 13.7 mmol) in anhydrous DMF (1 mL) were added 4-ethoxybenzyl chloride (2.81 g, 16.5 mmol) and potassium carbonate (3.78 g, 27.4 mmol) and the mixture was stirred at 50° C. overnight. Saturated brine was added thereto, and the mixture was extracted three times with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 1-{5-[(4-ethoxybenzyl)oxy]-1-benzofuran-2-yl}ethanone (6.95 g). This was directly used for the next reaction.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08501804B2 |
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| 出典データセット | uspto-grants-2013_08 |
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| ORD ID | ord-852283389d0e4a479baaeb76ed08dc28 |
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| 出典メモ | uspto-grants-2013_08 |
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