1,1,1-Trifluoro-5,5-dimethyl-2,4-hexanedione → 5-(tert-Butyl)-1-(4-nitrophenyl)-3-(trifluoromethyl)pyrazole
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3](=O)[CH2:4][C:5](=O)[C:6]([CH3:9])([CH3:8])[CH3:7].Cl.[N+:15]([C:18]1[CH:23]=[CH:22][C:21]([NH:24][NH2:25])=[CH:20][CH:19]=1)([O-:17])=[O:16]>>[C:6]([C:5]1[N:24]([C:21]2[CH:22]=[CH:23][C:18]([N+:15]([O-:17])=[O:16])=[CH:19][CH:20]=2)[N:25]=[C:3]([C:2]([F:13])([F:12])[F:1])[CH:4]=1)([CH3:9])([CH3:8])[CH3:7]Participants
3
Procedure
Using 1,1,1-trifluoro-5,5-dimethyl-2,4-hexanedione and 4-nitrophenylhydrazine hydrochloride as the raw materials, the same operation as the Example 538(1) gave the title compound.
Sources & evidence
- ORD record
- ord-eba3089427ee4a3697ff0375ed43d87f
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700655B2
Reaction notes
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