p-Fluoronitrobenzene → 4-(2H-1,2,3,4-tetrazol-2-yl)aniline

HRID 2278348

Reaktionsgleichung

Reaktionsgleichung von HRID 2278348
FC1C=CC([N+]([O-])=O)=CC=1.N1C=NN=N1.C(=O)([O-])[O-].[K+].[K+].N1(C2C=CC([N+]([O-])=O)=CC=2)C=NN=N1.[N:36]1[N:37]([C:41]2[CH:46]=[CH:45][C:44]([N+:47]([O-])=O)=[CH:43][CH:42]=2)[N:38]=[N:39][CH:40]=1>CN(C=O)C.C1COCC1.[Pt](=O)=O.O>[N:36]1[N:37]([C:41]2[CH:46]=[CH:45][C:44]([NH2:47])=[CH:43][CH:42]=2)[N:38]=[N:39][CH:40]=1

Komponenten

10

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of 4-fluoro-1-nitrobenzene (12.5 g, 89 mmol) and 1H-tetrazole (6.21 g, 89 mmol) in DMF (89 mL) stirred at room temperature, potassium carbonate (12.24 g, 89 mmol) was added in one portion. The resulting mixture was stirred at 80° C. overnight, and then reaction mixture was worked up by the addition of water at 80° C., then cooled to room temperature, and stirred at room temperature for 30 minutes. The yellow solid was collected by filtration, washed with water, air-dried for 2 hours, and dried in an vacuum oven at 60° C. for 2 hours to afford a mixture of 4-(1H-tetrazol-1-yl)-1-nitrobenzene and 4-(2H-tetrazol-2-yl)-1-nitrobenzene. The product thus obtained was re-dissolved in THF (209 mL) and, while stirring at room temperature, platinum(IV) oxide (0.45 g, 1.982 mmol) was added in one portion. The resulting mixture was stirred at room temperature overnight under a hydrogen atmosphere, after which the reaction mixture was worked up by filtration through a celite pad and the solvent removed by evaporation. The residue was purified and separated by CombiFlash® (0-50% EtOAc/toluene; Teledyne Isco, Inc., Lincoln, Nebr.) to afford the desired 4-(2H-tetrazol-2-yl)aniline as a yellowish solid. 1H NMR (400 MHz, DMSO-d6): δ 9.08 (s, 1H), 7.72 (d, 2H), 6.73 (d, 2H), 5.75 (s, 2H).

Aufarbeitung

  1. customreaction mixture
  2. temperaturecooled to room temperature
  3. stirringstirred at room temperature for 30 minutes
  4. filtrationThe yellow solid was collected by filtration
  5. washwashed with water
  6. customair-dried for 2 hours
  7. customdried in an vacuum oven at 60° C. for 2 hours
  8. customto afford
  9. customThe product thus obtained
  10. stirringwhile stirring at room temperature
  11. stirringThe resulting mixture was stirred at room temperature overnight under a hydrogen atmosphere
  12. filtrationafter which the reaction mixture was worked up by filtration through a celite pad
  13. customthe solvent removed by evaporation
  14. customThe residue was purified
  15. customseparated by CombiFlash® (0-50% EtOAc/toluene; Teledyne Isco, Inc., Lincoln, Nebr.)

Quellen und Nachweise

ORD-Eintrag
ord-ab33d0c5c1ee46eba7d23664771c01c1
Quelldatensatz
uspto-grants-2015_09
Patentnummer
US09133157B2

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