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Tetrahydrofuran → 4-(4-Dimethylaminomethyl-2-pyridyl)butylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-(3-Cyanopropyl)-4-dimethylaminomethylpyridine | HCID 13292607 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 4-(4-Dimethylaminomethyl-2-pyridyl)butylamine | HCID 20239072 | 100% |
反応手順
2-(3-Cyanopropyl)-4-dimethylaminomethylpyridine (1 g) in diethyl ether (15 ml) was added dropwise to a rapidly stirred suspension of lithium aluminium hydride (0.76 g) in ether (45 ml). The solution was stirred for 2.5 hours. Wet tetrahydrofuran, followed by 16% sodium hydroxide (1 ml) and then water was added and the mixture was filtered. The filtrate was evaporated to give 4-(4-dimethylaminomethyl-2-pyridyl)butylamine (1.02 g) as a clear oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04607107 |
| 出典データセット | uspto-grants-1986_08 |
| ORD ID | ord-334d2b24f54d4f5980bbea667f6222a7 |
| 出典メモ | uspto-grants-1986_08 |