関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Trimethylsilyl cyanide | HCID 82115 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 触媒 | zinc(II)iodide | HCID 9883512 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 13197589 | 68.4% |
反応手順
TMS-cyanide (8.52 mL, 68.1 mmol) was added to a solution of 6-methoxy-1-tetralone (6.0 g, 34 mmol) in toluene (50 mL). A trace amount (˜20 mg) of zinc iodide was added, and the reaction was stirred at 60° C. for 16 hours. The solution was cooled to rt and diluted with THF (30 mL). This was added to a mixture of lithium aluminum hydride (2.58 g) in THF (50 mL), and the reaction mixture was heated at 42° C. for 2 h. The reaction was cooled to rt. EtOAc (10 mL) was slowly added, and the reaction stirred 30 min. Water (2 mL) and then 5N NaOH (1 mL) were slowly added, and the reaction stirred 1 h. The reaction mixture was diluted with EtOAc (100 mL), dried (MgSO4), and filtered through Celite. Purification by silica gel chromatography (10-20% MeOH/DCM) gave 4.82 g of 1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a clear oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09447045B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-060b901605a7488ead9bd01c7620fa71 |
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| 出典メモ | uspto-grants-2016_09 |
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