Water → 2-(2,6-dichloro-4-trifluoromethylphenyl)-2H-1,2,3-triazole-4-carboxylic acid
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([Cl:12])[C:3]=1[N:13]1[N:17]=[C:16]([CH:18]=[O:19])[CH:15]=[N:14]1.[OH2:20]>S(=O)(=O)(O)O.[O-2].[O-2].[O-2].[Cr+6]>[Cl:12][C:4]1[CH:5]=[C:6]([C:8]([F:11])([F:9])[F:10])[CH:7]=[C:2]([Cl:1])[C:3]=1[N:13]1[N:17]=[C:16]([C:18]([OH:20])=[O:19])[CH:15]=[N:14]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2-(2,6-dichloro-4-trifluoromethylphenyl)-2H-1,2,3-triazole-4-carboxaldehyde (1 g) was oxidised using chromium trioxide (26.67 g) in water (40 ml) and concentrated sulphuric acid (23 ml), made up to 100 ml. The product was extracted with ether and worked up in conventional manner to give 2-(2,6-dichloro-4-trifluoromethylphenyl)-2H-1,2,3-triazole-4-carboxylic acid, m.p. 155°-157°.
Workup
- extractionThe product was extracted with ether
Sources & evidence
- ORD record
- ord-f3615841c3614c63a8851a9a5172e9cc
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05064844
Reaction notes
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