Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cycloheptylamine → N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cycloheptylamine | HCID 2899 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Methylphenanthrene | HCID 17321 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine | HCID 15284290 | 66.9% |
반응 단계
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)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05420348 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-b2325b9e98944fdc89b7e22fd4005c14 |
| 출처 메모 | uspto-grants-1995_05 |