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Borane;tetrahydrofuran → Methyl 3-(piperidin-1-yl)benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Borane;tetrahydrofuran | HCID 2723981 | — |
| 反応物 | Methyl 3-(2-oxopiperidin-1-yl)benzoate | HCID 10681135 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 3-(piperidin-1-yl)benzoate | HCID 7148413 | 90% |
反応手順
The compound of Example 37 (640 mg, 2.75 mmol) was dissolved in dry THF (30 ml) and borane-tetrahydrofuran complex (5 ml, 1M solution in THF) was added. The mixture was stirred under nitrogen under reflux for 1 h, then cooled and evaporated. The residue was taken up in MeOH/acetic acid (6/1, v/v, 70 ml) and heated under reflux for 3 h, then evaporated and chromatographed (eluant 10% EtOAc in hexanes) to provide a colourless oil (540 mg, 90%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728829 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-b2a2fb45af4f44099c49615f8d09865c |
| 出典メモ | uspto-grants-1998_03 |