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Water → 1-(4-Nitrophenyl)-1H-1,2,4-triazole

HRID 2392670
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HRID 2392670 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[NH:11]1[CH:15]=[N:14][CH:13]=[N:12]1.C(=O)([O-])[O-].[K+].[K+].O>CS(C)=O>[N:11]1([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=2)[CH:15]=[N:14][CH:13]=[N:12]1
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참가 물질

6

반응물 4

HCID 962WaterHCID 92571H-1,2,4-TriazoleHCID 9590p-FluoronitrobenzeneHCID 11430Potassium Carbonate

생성물 1

HCID 110953981-(4-Nitrophenyl)-1H-1,2,4-triazole

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
90 °C

실험 절차

4Fluoronitrobenzene (2 g, 0.014 mol), 1,2,4-triazole (1 g, 0.014 mol), potassium carbonate (1.96 g, 0.014 mol) were dissolved in DMSO (50 ml) and stirred at 90° C. for 24 h under dry conditions. The yellow suspension was poured into water (150 ml), extracted (EtOAc), dried (Na2SO4) and evaporated under reduced pressure to afford an orange solid which was purified by flash column chromatography on silica eluting with n-pentane/ethyl acetate (50-100%) to afford a white solid (2.57 g 97%).

후처리

  1. extractionextracted (EtOAc)
  2. dry with materialdried (Na2SO4)
  3. customevaporated under reduced pressure
  4. customto afford an orange solid which
  5. customwas purified by flash column chromatography on silica eluting with n-pentane/ethyl acetate (50-100%)
  6. customto afford a white solid (2.57 g 97%)

출처 및 근거

ORD 기록
ord-a98078005de946f7bbb9ee7c31a04b54
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05801170

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