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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926853생성일: 2026년 10월 24일

Potassium Carbonate → 1-(3,4-dimethylphenyl)-3-nitro-1H-pyrazole

https://huagongshe.com/ko/reaction/926853

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Bromo-o-xyleneHCID 68504—
반응물L-ProlineHCID 145742—
반응물HCID 178526745HCID 178526745—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-(3,4-dimethylphenyl)-3-nitro-1H-pyrazoleHCID 665875049%

반응 조건

온도85 °C

반응 단계

Into a 250-mL round bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-nitro-1H-pyrazole (6 g, 53.10 mmol, 1.00 equiv) in DMSO (80 mL), 4-bromo-1,2-dimethylbenzene (11.8 g, 64.13 mmol, 1.21 equiv), CuI (1.6 g, 8.42 mmol, 0.16 equiv), L-proline (1 g, 8.70 mmol, 0.16 equiv), and potassium carbonate (14.6 g, 105.80 mmol, 1.99 equiv). The resulting solution was stirred overnight at 85° C. in an oil bath. The reaction progress was monitored by LCMS. The resulting solution was diluted with 300 mL of water. The resulting solution was extracted with 4×100 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 3×100 mL of water and 1×100 mL of brine. The mixture was dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1:10) to give 1 g (9%) of 1-(3,4-dimethylphenyl)-3-nitro-1H-pyrazole as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09289430B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-be3f983de45e4e2581df79a4ea9ecf7e
출처 메모uspto-grants-2016_03