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Ethanol → 4-Amino-3-(benzylthio)-3-methylbutan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 反応物 | 3-(Benzylthio)-3-methyl-4-nitrobutan-1-ol | HCID 57475976 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Amino-3-(benzylthio)-3-methylbutan-1-ol | HCID 57475977 | 99% |
反応手順
To a mixture of lithium aluminum hydride (1.67 g) and tetrahydrofuran (30 ml) was added a solution of 3-(benzylthio)-3-methyl-4-nitrobutan-1-ol (3.00 g) in tetrahydrofuran (10 ml) over 1 hr at room temperature. The reaction mixture was stirred at room temperature for 1 hr, ethanol (10 ml) and water (6.4 ml) were added in this order, and the resulting inorganic salt was removed by filtration. The filtrate was concentrated, and the residue was dissolved in ethyl acetate, dried (MgSO4), and concentrated to give the title compound (2.62 g, yield 99%) as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08410087B2 |
| 出典データセット | uspto-grants-2013_04 |
| ORD ID | ord-e9bf906186a04b8d8b87ef23067b4ed6 |
| 出典メモ | uspto-grants-2013_04 |