Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanol → 1-(5-Methoxy-2-nitro-phenyl)-piperidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 1-(5-Chloro-2-nitrophenyl)piperidine | HCID 3096079 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-(5-Methoxy-2-nitro-phenyl)-piperidine | HCID 69310428 | 41% |
반응 단계
To 1-(5-chloro-2-nitro-phenyl)-piperidine (197 mg, 0.810 mmol) in 1.5 mL of DMF was added 4 mL of 0.5 M NaOMe in MeOH (2.5 eq). The resultant solution was heated at 60° C. overnight, then at 90° C. for 24 h. The reaction was diluted with EtOAc (50 mL) and washed with water (50 mL), dried (Na2SO4) and concentrated in vacuo. Purification by preparative TLC (20% EtOAc-hexane) gave 80 mg (41%) of the title compound, along with 80 mg (40%) of recovered starting material. 1H-NMR (CDCl3; 400 MHz): δ 7.95 (d, 1H, J=9.1 Hz), 6.51 (d, 1H, J=2.6 Hz), 6.46 (dd, 1H, J=2.6, 9.1 Hz), 3.87 (s, 3H), 3.01-3.04 (m, 4H), 1.72-1.78 (m, 4H), 1.60-1.64 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07427683B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-4415a01d13f14a71a7183f8e8589ba6a |
| 출처 메모 | uspto-grants-2008_09 |