Nitric Acid → 2-(p-Chlorophenyl)-3-nitro-5[(trifluoromethyl)thio]pyrrole
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:9][C:10]([S:13][C:14]([F:17])([F:16])[F:15])=[CH:11][CH:12]=2)=[CH:4][CH:3]=1.[N+:18]([O-:21])([OH:20])=[O:19]>C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10]([S:13][C:14]([F:15])([F:17])[F:16])=[CH:11][C:12]=2[N+:18]([O-:20])=[O:19])=[CH:6][CH:7]=1.[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10]([S:13][C:14]([F:16])([F:15])[F:17])=[C:11]([N+:18]([O-:21])=[O:19])[CH:12]=2)=[CH:6][CH:7]=1Participants
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(p-chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole (1.0 g, 0.0036 mol) in acetic acid is cooled with an ice bath, treated with nitric acid (0.24 g, 0.00378 mol), stirred for two hours, poured into ice-water and stirred for one hour. The aqueous solution is filtered and the filter cake is washed with water and dried in a vacuum dessicator to obtain a tan solid. Flash chromatography of the solid using silica gel and a 1:10 ethyl acetate/hexanes solution gives 2-(p-chlorophenyl)-3-nitro-5-[(trifluoromethyl)thio]pyrrole as a yellow solid (0.45 g, mp 143°-145° C.) and 5-(p-chlorophenyl)-3-nitro-2-[(trifluoromethyl)thio]pyrrole as a yellow solid (0.17 g, mp 185°-193° C.) Both products are identified by 1HNMR, 19FNMR and 13CNMR spectral analyses.
Workup
- stirringstirred for one hour
- filtrationThe aqueous solution is filtered
- washthe filter cake is washed with water
- customdried in a vacuum dessicator
- customto obtain a tan solid
Sources & evidence
- ORD record
- ord-edeb24584db443339fb8b432d18767c9
- Source dataset
- uspto-grants-1994_02
- Patent number
- US05284863
Reaction notes
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