Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylformamide → 5-methyl-3-(4-methyl-3-nitro-phenyl)-1H-pyrazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 3'-Nitro-4'-methylacetophenone | HCID 79246 | — |
| 반응물 | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| 생성물 | 5-methyl-3-(4-methyl-3-nitro-phenyl)-1H-pyrazole | HCID 59377531 | — |
반응 단계
A solution of 1-(4-methyl-3-nitro-phenyl)-ethanone and (1,1-dimethoxy-ethyl)-dimethyl-amine in DMF was heated at 90° C. for 3 hours, then cooled to room temperature. Solvent was removed under reduced pressure, and the residue was dissolved in a mixture of EtOH (25 ml) and THF (5 ml). The mixture was cooled to 0° C., and hydrazine hydrate (5 ml) at 0° C. was added. The mixture was stirred for 16 hours at room temperature, then concentrated under reduced pressure. The residue was purified by “flash chromatography” (0 to 30% EtOAc in hexanes) to give 8.5 g of 5-methyl-3-(4-methyl-3-nitro-phenyl)-1H-pyrazole as a yellowish solid, which was recrystallyzed from EtOAc to give 8.2 g of yellow powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08871760B2 |
| 출처 데이터셋 | uspto-grants-2014_10 |
| ORD ID | ord-db45aec6d893439587875242df22e5c5 |
| 출처 메모 | uspto-grants-2014_10 |