関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1'-benzyl-5-chloro-3H-spiro[isobenzofuran-1,4'-piperidin]-3-one | HCID 59833643 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1'-Benzyl-5-chloro-3H-spiro[isobenzofuran-1,4'-piperidine] | HCID 59833632 | 95.1% |
反応手順
To a solution of 1′-benzyl-5-chloro-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one (1.1 g, 3.35 mmol) in THF (12 mL) was added 1 M solution of borane complex in THF (7 mL, 7.0 mmol) slowly at 0° C. After addition was complete reaction mixture was kept at room temperature for 30 min, then kept at reflux overnight, cooled to 0° C. and 6M aqueous HCl (3.5 mL) was added slowly. The reaction mixture was kept at reflux for 5 h, cooled to 0° C., pH of the reaction mixture was adjusted to 10 by addition of aqueous NaOH (6M) and the whole was extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulphate (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel flash chromatography (0-30% ethyl acetate in petroleum ether) to give the subtitled compound (1.0 g).
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-4fa3fb46812240c59a78ebdd85624430 |
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| 出典メモ | uspto-grants-2008_11 |
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