Nitric Acid → HCID 178526837, compound

HRID 2196967Notes

Reaction equation

HRID 2196967 reaction equation
[OH:1][C:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][N:3]=1.S(=O)(=O)(O)O.[N+:17]([O-])([OH:19])=[O:18]>>[N+:17]([C:5]1[CH:6]=[C:7]([C:8]([F:9])([F:11])[F:10])[C:2]([OH:1])=[N:3][CH:4]=1)([O-:19])=[O:18]

Participants

4

Conditions

Temperature
50 °C

Procedure

2-Hydroxy-3-(trifluoromethyl)pyridine (3.0 g) was added to conc. sulfuric acid (18 mL) under ice-cooling, and the mixture was stirred at the same temperature for 5 min. Fuming nitric acid (90-95%, 7 mL) was added dropwise over 5 min, and the mixture was allowed to return to room temperature over 2 hr, heated to 50° C. and stirred for 3 hr. After cooling to room temperature, the reaction mixture was poured into ice (200 g), and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The precipitate was washed with diisopropyl ether to give the title compound as a solid (yield 2.7 g, 69%).

Workup

  1. temperaturecooling
  2. waitto return to room temperature over 2 hr
  3. stirringstirred for 3 hr
  4. temperatureAfter cooling to room temperature
  5. extractionthe mixture was extracted with ethyl acetate
  6. washThe extract was washed with saturated brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. washThe precipitate was washed with diisopropyl ether

Sources & evidence

ORD record
ord-580e368d409a4fe2841dec78c13ba08c
Source dataset
uspto-grants-2012_12
Patent number
US08338461B2

Reaction notes

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