化工社化工社 化学情報印刷レポート · 研究参考用
Cycloheptylamine → N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cycloheptylamine | HCID 2899 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Methylphenanthrene | HCID 17321 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine | HCID 15284290 | 66.9% |
反応手順
2-Methylphenanthrene (2.00 g, 10.4 mmol) was brominated with N-bromosuccinimide (2.05 g, 11.5 mmol) and the product compound was added gradually to a suspension of cycloheptylamine (2.38 g, 21.0 mmol) and potassium carbonate (2.90 μg, 21.0 mmol) in dimethylformamide (20 ml) with ice-cooling. The mixture was then stirred at room temperature for 16 hrs and, then, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2.11 g of a viscous liquid. 1H-NMR (δ ppm, in deuteriochloroform) 2.83 (2H, m), 4.02 (2H, s), 8.68 (2H, m)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05420348 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-b2325b9e98944fdc89b7e22fd4005c14 |
| 出典メモ | uspto-grants-1995_05 |