Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Bromopropiophenone → 2-{[4-(2-Hydroxyethyl)phenyl]amino}-1-phenyl-1-propanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Bromopropiophenone | HCID 16452 | — |
| 반응물 | 4-Aminophenethyl alcohol | HCID 66904 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-{[4-(2-Hydroxyethyl)phenyl]amino}-1-phenyl-1-propanone | HCID 22291349 | — |
반응 단계
A mixture of 4-aminophenethyl alcohol (690 mg, 5.0 mmol), 2-bromopropiophenone (2.1 g, 10 mmol) potassium carbonate (690 mg, 5.0 mmol) in DMF (50 mL) was stirred at ambient temperature for 3 days. The mixture was partitioned between ethyl acetate and water. The combined organic phase was dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel eluting with hexane/ethyl acetate (2:1) to afford the title compound quantitatively as yellow oil: 1H-NMR (CDCl3) δ 1.49 (2H, d, J=6.9 Hz), 2.74 (2H, t, J=6.4 Hz), 3.79 (2H, t, J=6.4 Hz), 4.65 (1H, br), 5.11 (1H, m), 6.65 (2H, d, J=8.4 Hz), 7.05 (2H, d, J=8.6 Hz), 7.48-7.65 (3H, m), 8.03 (2H, d, J=7.2 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06956050B2 |
| 출처 데이터셋 | uspto-grants-2005_10 |
| ORD ID | ord-e0161847907e49918ace3ffa7c8d46f4 |
| 출처 메모 | uspto-grants-2005_10 |