Nitric Acid → HCID 178526837, compound
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) and nitric acid (1.644 mL, 36.8 mmol) was added 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 and 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
- temperatureThe mixture was then warmed to 60° C. for 5 h
- temperaturecooled
- extractionThe mixture was extracted with EA (2×100 mL)
- washwashed with H2O (100 mL)
- customto give the organic layer
- extractionThe combined organic extract
- washwas washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-a9ddbcf0a8de469b9f08b4cce64d6017
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937071B2
Reaction notes
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