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Tetrahydrofuran → (1-Benzyl-4-piperidyl)methanamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | N-benzylpiperidine-4-carboxamide | HCID 3868064 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 生成物 | (1-Benzyl-4-piperidyl)methanamine | HCID 1514444 | — |
反応手順
To a solution of N-benzylisonipecotamide (7.34g, 34 mmol) in 60 mL of anhydrous THF, was added, LiAlH4 (1.9 g, 51 mmol) and the mixture was stirred at room temperature for 10 minutes followed by heating to reflux for 3 h. The reaction was quenched by addition of 100 mL sat'd. sodium potassium tartrate, and was extracted with EtOAc (3×50 mL). The combined extracts were washed with 20 mL water and 20 mL brine then dried over MgSO4, filtered and concentrated to give the desired product. 1H-NMR (400 MHz, CDCl3) δ7.13 (m, 5H), 3.42 (s, 2H), 2H), 2.91 (m, 2H), 2.59 (m, 2H), 1.97 (m, 2H), 1.62 (m, 2H), 2.21 (m, 5H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07067506B2 |
| 出典データセット | uspto-grants-2006_06 |
| ORD ID | ord-5853d05e12d34035b74547b4333db766 |
| 出典メモ | uspto-grants-2006_06 |