Sulfolane → 2-Fluoro-5-nitropyridine

HRID 1357771Notes

Reaction equation

HRID 1357771 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7](Cl)=[N:8][CH:9]=1)([O-:3])=[O:2].[F-:11].[K+].C1CS(=O)(=O)CC1>C1C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([F:11])=[N:8][CH:9]=1)([O-:3])=[O:2]

Participants

5

Procedure

A mixture of 5-nitro-2-chloropyridine (2.0 g, 12.6 mmol) and anhydrous potassium fluoride (2.2 g, 38 mmol) in a combination of sulfalone (6 mL) and benzene (4 mL) was stirred at RT for 20 min. The benzene was then removed by distillation. The resulting mixture was heated at 150° C. for 12 h. The mixture was cooled to RT whereupon water (60 mL) was added. The desired product was separated from the solution via steam distillation. Extraction of the distillate with diethyl ether (2×10 mL) followed by drying (Na2SO4) and concentration gave 5-nitro-2-fluoropyridine as a water white oil (1.3 g, 73%).

Workup

  1. customThe benzene was then removed by distillation
  2. temperatureThe resulting mixture was heated at 150° C. for 12 h
  3. temperatureThe mixture was cooled to RT whereupon water (60 mL)
  4. additionwas added
  5. customThe desired product was separated from the solution via steam distillation
  6. extractionExtraction of the distillate with diethyl ether (2×10 mL)
  7. customby drying
  8. concentration(Na2SO4) and concentration

Sources & evidence

ORD record
ord-46a403b72a134566aa692b63e8722101
Source dataset
uspto-grants-2003_07
Patent number
US06593349B2

Reaction notes

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