関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol | HCID 59833635 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1'-benzyl-5-methyl-3H-spiro[1-benzofuran-2,4'-piperidine] | HCID 59833633 | 41% |
反応手順
To a suspension of NaH (55% in mineral oil, 200 mg, 5 mmol) in toluene (10 mL) was slowly added a solution of crude 1-benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol in toluene (15 mL). After addition was completed, the reaction mixture was heated to 110° C. and stirred for 5 min. DMF (9 mL) was added and stirring was continued at reflux temperature for 10 h. The reaction mixture was cooled to room temperature, poured into water (50 ml), and extracted with ethyl acetate (2×25 ml). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (ethyl acetate/n-heptane) to give the subtitle compound (240 mg, 41%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07449475B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-260f62b0aab84857b4fdc4e95d4293a3 |
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| 出典メモ | uspto-grants-2008_11 |
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