Benzene, 1-bromo-3-nitro- → HCID 86653354, compound
Reaction equation
CC1(C)C(C)(C)OB([C:9]2[CH:10]=[N:11][N:12]([C:14]([OH:16])=[O:15])[CH:13]=2)O1.Br[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([N+:25]([O-:27])=[O:26])[CH:20]=1>>[N+:25]([C:21]1[CH:20]=[C:19]([C:9]2[CH:10]=[N:11][N:12]([C:14]([OH:16])=[O:15])[CH:13]=2)[CH:24]=[CH:23][CH:22]=1)([O-:27])=[O:26]Participants
3
Procedure
Using the same method as in Example 5-(i), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylic acid.tert-butyl was reacted with 1-bromo-3-nitrobenzene to give 4-(3-nitrophenyl)-1H-pyrazole-1-carboxylic acid.tert-butyl (yield: 64%).
Sources & evidence
- ORD record
- ord-50ba3b121afb43bba62633d6eaae4716
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415479B2
Reaction notes
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