Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(4-Nitrophenyl)hydrazine → 1-(4-Nitrophenyl)-3,5-diphenylpyrazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (4-Nitrophenyl)hydrazine | HCID 3310889 | — |
| 반응물 | Phenylbenzylglyoxal | HCID 11096234 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-(4-Nitrophenyl)-3,5-diphenylpyrazole | HCID 680475 | 76.2% |
반응 단계
In a 500-ml four-necked flask were placed 22.4 g (0.10 mole) of 1,3-diphenylpropanedione, 20.0 g (0.13 mole) of p-nitrophenylhydrazine, and 200.7 g of toluene. The mixture was then heated under reflux with stirring for three hours. Upon completion of the reaction, the reaction mixture was cooled to room temperature and a solid was recovered by filtration. The filtrate was concentrated under reduced pressure to dryness. The residue was purified by reslurrying by adding 300 ml of methanol. Thereafter, the residue was cooled to room temperature and a solid was recovered by filtration. The solid was washed with methanol and dried under reduced pressure to give 26.0 g of 1-(p-nitrophenyl)-3,5-diphenylpyrazole.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07816020B2 |
| 출처 데이터셋 | uspto-grants-2010_10 |
| ORD ID | ord-cc5f974fd503400884c4c30e4533d688 |
| 출처 메모 | uspto-grants-2010_10 |