Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 1-(5-Chloro-2-methyl-4-nitrophenyl)-3-methylpyridin-2(1H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-Chloro-2-fluoro-5-nitrotoluene | HCID 87593 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | HCID 178426317 | HCID 178426317 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(5-Chloro-2-methyl-4-nitrophenyl)-3-methylpyridin-2(1H)-one | HCID 59586695 | — |
반응 단계
1.50 g (13.8 mmol) of 2-hydroxy-3-methylpyridine in 70 ml of DMF are admixed at 0° C. with 2.31 g (20.6 mmol) of potassium tert-butoxide, and the mixture is stirred at room temperature for 30 min. 2.87 g (15.1 mmol) of 2-chloro-4-fluoro-5-methylnitrobenzene are added while continuing to stir at RT. After 17 h, the mixture is admixed with 1000 ml of water and then extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulfate and, after filtration, the solvents are removed under reduced pressure. The residue is purified by chromatography on silica gel (2:1 cyclohexane/ethyl acetate). This affords 2.15 g (56% of theory) of the desired compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08198267B2 |
| 출처 데이터셋 | uspto-grants-2012_06 |
| ORD ID | ord-babfbf2138ce4c39855e0fa8fe8bc918 |
| 출처 메모 | uspto-grants-2012_06 |