Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Nitropropane → 7-bromo-5-chloro-1H-indole-3-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Nitropropane | HCID 7903 | — |
| 반응물 | Ammonium phosphate, tribasic | HCID 159282 | — |
| 반응물 | 7-bromo-5-chloro-1H-indole-3-carbaldehyde | HCID 57546113 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 7-bromo-5-chloro-1H-indole-3-carbonitrile | HCID 57546220 | 54.5% |
반응 단계
A mixture of 7-bromo-5-chloro-1H-indole-3-carbaldehyde (0.80 g, 3.09 mmol), Ammonium phosphate, dibasic (1.269 mL, 15.47 mmol), and 1-nitropropane (0.276 mL, 3.09 mmol) in Acetic Acid (20 mL) was heated at reflux. The solvent was evaporated, the residue was taken up in aqueous sodium bicarbonate (300 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were dried with MgSO4 and evaporated. The residue was purified by chromatography on SiO2 with 20%-25% ethyl acetate/hexanes to give 7-bromo-5-chloro-1H-indole-3-carbonitrile (0.43 g, 1.683 mmol, 54.4% yield) as a yellow solid. 1H-NMR (CDCl3, 400 MHz) δ 8.27 (bs, 1H), 7.79 (s, 1H), 7.72 (d, J=1.8 Hz, 1H), 7.49 (d, J=1.8 Hz, 1H). LC/MS (HPLC method 4): tR=3.12 min, 255.01(MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08026257B2 |
| 출처 데이터셋 | uspto-grants-2011_09 |
| ORD ID | ord-b014e68c04824017b8e7a4fd2023d96d |
| 출처 메모 | uspto-grants-2011_09 |