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1,2-Difluoro-4-nitrobenzene → 1-(2-fluoro-4-nitrophenyl)-5-methyl-1H-1,2,4-triazole

HRID 1855499
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HRID 1855499 반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:6][C:7]=1F.[CH3:12][C:13]1[N:17]=[CH:16][NH:15][N:14]=1.O.O.O.P([O-])([O-])(O)=O.[K+].[K+]>CS(C)=O>[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:6][C:7]=1[N:14]1[C:13]([CH3:12])=[N:17][CH:16]=[N:15]1
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참가 물질

5

반응물 3

HCID 1230531,2-Difluoro-4-nitrobenzeneHCID 16217523Potassium phosphate, dibasic, trihydrateHCID 178433329HCID 178433329, 화합물

생성물 1

HCID 584144611-(2-fluoro-4-nitrophenyl)-5-methyl-1H-1,2,4-triazole수율 22.3%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

3,4-Difluoronitrobenzene (514 mg, 3.23 mmol), 3-methyl-1H-1,2,4-triazole (325 mg, 3.72 mmol) and di-potassium hydrogen phosphate trihydrate (1.49 g, 6.46 mmol) in dimethyl sulfoxide (1.5 mL) were stirred for 6 hours at 70° C. The mixture was concentrated in vacuo; the residue was diluted in water and extracted three times with ethyl acetate. The combined organic layers were washed four times with water, twice with brine, dried with magnesium sulfate and evaporated. Column chromatography (30 g silica, heptane/ethyl acetate 1:1 v/v) afforded the title compound (160 mg, 22%) as white crystals MS ISP (m/e): 223.2[(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=8.22 (m, 2H), 8.04 (s, 1H), 7.74 (dd, 1H), 2.48 (d, 3H). Mp 56-58° C.

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. additionthe residue was diluted in water
  3. extractionextracted three times with ethyl acetate
  4. washThe combined organic layers were washed four times with water
  5. dry with materialtwice with brine, dried with magnesium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-f0deee69c8ae40d2a8e717f6d33a05d1
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962834B2

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