Nitric Acid → HCID 22618355, compound
Reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:17])([F:16])[F:15])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]([F:22])([F:21])[F:20])[CH:3]=1.[N+:23]([O-])([OH:25])=[O:24]>S(=O)(=O)(O)O.C(OCC)(=O)C.CCCCCC>[NH2:1][C:2]1[N:6]([C:7]2[C:8]([Cl:18])=[CH:9][C:10]([C:14]([F:15])([F:16])[F:17])=[CH:11][C:12]=2[Cl:13])[N:5]=[C:4]([C:19]([F:22])([F:21])[F:20])[C:3]=1[N+:23]([O-:25])=[O:24]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole (3.0 g) in concentrated sulphuric acid (10 ml) at 0° C. was treated with fuming nitric acid (9 ml) during 15 minutes, keeping the temperature at 5°-15° C. After 30 minutes the mixture was poured onto excess ice, and the precipitated solid was filtered off and dissolved in ethyl acetate. After drying over anhydrous magnesium sulphate, filtration, and evaporation in vacuo a brown oil was obtained. This oil was dissolved in the minimum of ethyl acetate and diluted with hexane. A pale yellow solid crystallized and this was discarded. The filtrate was evaporated in vacuo to give a solid which was recrystallized from toluene-hexane to furnish a yellow solid. One further recrystallization from the same solvent pair gave 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-nitro-3-trifluoromethylpyrazole as white crystals, m.p. 214°-215° C.
Workup
- customat 5°-15° C
- additionAfter 30 minutes the mixture was poured onto excess ice
- filtrationthe precipitated solid was filtered off
- dissolutiondissolved in ethyl acetate
- dry with materialAfter drying over anhydrous magnesium sulphate, filtration, and evaporation in vacuo a brown oil
- customwas obtained
- customA pale yellow solid crystallized
- customThe filtrate was evaporated in vacuo
- customto give a solid which
- customwas recrystallized from toluene-hexane
- customto furnish a yellow solid
- customOne further recrystallization from the same solvent pair
Sources & evidence
- ORD record
- ord-15e19be994ca4c6c8fa9748f8c4c0716
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05714191
Reaction notes
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