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4-Aminocyclohexanecarboxylic acid → ((1s,4s)-4-Aminocyclohexyl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Aminocyclohexanecarboxylic acid | HCID 171560 | — |
| 反応物 | Borane;tetrahydrofuran | HCID 2723981 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | ((1s,4s)-4-Aminocyclohexyl)methanol | HCID 424390 | 78% |
反応手順
To a solution of (1r,4r)-4-aminocyclohexanecarboxylic acid (860 mg, 6.0 mmol, 1.0 eq) in THF (10 mL) was added dropwise BH3/THF (1.0 mol/L in THF, 30 mL, 5.0 equiv.) at 0° C. The reaction was allowed to warm to room temperature. The reaction was heated at reflux for 48 hours. The reaction was quenched with AcOH and concentrated in vacuo to get crude ((1r,4r)-4-aminocyclohexyl)methanol (600 mg, 78%) which was used to the next step without further purification. MS: m/z 130.1 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09340554B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-3e7a5d5f5a934d9188e5ee27d474ea8e |
| 出典メモ | uspto-grants-2016_05 |