Nitrogen → 4-(4-Fluorophenoxy)-1-methyl-2-nitrobenzene

HRID 1769879

反応式

HRID 1769879 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[F:12][C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+].N#N>CCOCC.N1C=CC=CC=1>[N+:9]([C:4]1[CH:3]=[C:2]([O:19][C:16]2[CH:17]=[CH:18][C:13]([F:12])=[CH:14][CH:15]=2)[CH:7]=[CH:6][C:5]=1[CH3:8])([O-:11])=[O:10]

参加物

7

反応条件

温度
90 °C

実験手順

4-Bromo-2-nitrotoluene (25.0 g, 116 mmol), 4-fluorophenol (8.70 g, 77.6 mmol), potassium carbonate (21.5 g, 156 mmol) and pyridine (75 mL), were combined under N2 atmosphere and heated at 90° C. for 30 min. The reaction mixture was cooled to ambient temperature, CuO (15.4 g, 194 mmol) was added under a stream of N2, and the resulting dark-brown suspension was heated at reflux for 17 hours. The reaction mixture was cooled to ambient temperature and diluted with ether. The solids were removed by filtration through celite. The ethereal solution was washed with 1.0M aqueous NaOH, 1.0M aqueous HCl and brine, dried over Na2SO4, filtered and concentrated in vacuo to give a dark-brown oil. The crude product was purified by chromatography on silica gel to give 2-nitro-4-(4-fluorophenoxy)-toluene (12.1 g, 63%).

後処理

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. temperaturethe resulting dark-brown suspension was heated
  3. temperatureat reflux for 17 hours
  4. temperatureThe reaction mixture was cooled to ambient temperature
  5. customThe solids were removed by filtration through celite
  6. washThe ethereal solution was washed with 1.0M aqueous NaOH, 1.0M aqueous HCl and brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customto give a dark-brown oil
  11. customThe crude product was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-617fa578f2bb4f928045873af01b8827
出典データセット
uspto-grants-1995_01
特許番号
US05382670

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