Nitric Acid → HCID 178526837, compound

HRID 1428547Notes

Reaction equation

HRID 1428547 reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[C:4]([OH:9])=[N:5][CH:6]=[CH:7][CH:8]=1.[N+:12]([O-])([OH:14])=[O:13].OS(O)(=O)=O>>[N+:12]([C:7]1[CH:8]=[C:3]([C:2]([F:1])([F:10])[F:11])[C:4]([OH:9])=[N:5][CH:6]=1)([O-:14])=[O:13]

Participants

4

Conditions

Temperature
25 °C

Procedure

To a mixture of 3-(trifluoromethyl)pyridin-2-ol (2 g, 12.26 mmol) was added nitric acid (1.644 mL, 36.8 mmol) and H2SO4 (12.03 g, 123 mmol) at 0° C. Then the mixture was stirred at 25° C. for 16 h. The mixture was then warmed to 60° C. for 5 h, cooled and added to 150 g of ice. The mixture was extracted with EA (2×100 mL) and washed with H2O (100 mL) to give the organic layer. The combined organic extract was washed with brine, dried over Na2SO4, concentrated to yield a brown solid of 5-nitro-3-(trifluoromethyl)pyridin-2-ol (2.2 g, 8.99 mmol, 73.3% yield): 1H NMR (400 MHz, CD3OD) δ 8.91 (d, J=2.43 Hz, 1H), 9.42 (d, J=2.43 Hz, 1H); ES-LCMS m/z 209.0 (M+H).

Workup

  1. temperatureThe mixture was then warmed to 60° C. for 5 h
  2. temperaturecooled
  3. extractionThe mixture was extracted with EA (2×100 mL)
  4. washwashed with H2O (100 mL)
  5. customto give the organic layer
  6. extractionThe combined organic extract
  7. washwas washed with brine
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-1aee7c310cb847bc9da66bb77dad28d1
Source dataset
uspto-grants-2015_01
Patent number
US08937071B2

Reaction notes

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