Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Quinoline → 2-Chloro-5-(trifluoromethyl)nicotinonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Quinoline | HCID 7047 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2-Oxo-5-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile | HCID 14837020 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-Chloro-5-(trifluoromethyl)nicotinonitrile | HCID 20071599 | — |
반응 단계
To a mixture of phosphorous oxychloride (13.4 mL, 144 mmol) and quinoline (8.7 mL, 73 mmol) was added the product from Step C above (24.6 g, 131 mmol) and the resultant mixture was heated to reflux for 3 h. The reaction was cooled to 100° C. before water (70 mL) was slowly added. The mixture was further cooled to room temperature and neutralized by the cautious addition of saturated aqueous sodium bicarbonate solution. The aqueous layer was extracted with three portions of ethyl acetate and the organic layers were combined, dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography to afford the desired compound. 1H NMR (500 MHz, CDCl3) δ 8.88 (d, J=2.0 Hz, 1H), 8.26 (d, J=2.5 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07388019B2 |
| 출처 데이터셋 | uspto-grants-2008_06 |
| ORD ID | ord-15754b359c6e4374b7dbfa22f34c8819 |
| 출처 메모 | uspto-grants-2008_06 |