Reaction equation
FC(F)(F)C(OI(C1C=CC=CC=1)O[C:8](=[O:13])C(F)(F)F)=O.B(F)(F)F.CCOCC.[CH3:31][CH2:32][O:33][C:34]([C:36]([CH2:38][C:39]([C:41]([CH3:44])([CH3:43])[CH3:42])=O)=O)=[O:35].[CH3:45][NH:46][NH2:47]>CO>[CH2:32]([O:33][C:34]([C:36]1[N:46]([CH3:45])[N:47]=[C:39]([C:41]([CH3:42])([CH3:43])[CH3:44])[C:38]=1[O:13][CH3:8])=[O:35])[CH3:31]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
[Bis(trifluoroacetoxy)iodo]benzene (430 mg, 1.00 mmol) was dissolved in anhydrous MeOH (4 mL), the resulting solution was stirred at room temperature for 3 min. BF3.OEt2 (0.123 mL, 1.00 mmol) was then added via syringe. Ethyl trimethylacetopyruvate (200 mg, 1.00 mmol) was added dropwise via syringe and the resulting mixture was stirred at room temperature for 12 h. The solvent was removed under reduced pressure and the resulting residue was dissolved in dry EtOH (2 mL). CH3NHNH2 (52.6 μL, 1.00 mmol) was added via syringe and the resulting mixture was stirred at 80° C. for 8 h. The solvent was removed under reduced pressure and the resulting residue was chromatographed on a 24-g SiO2 pre-packed column eluting with 0:1-3:7 EtOAc/hexanes to yield 5-tert-butyl-4-methoxy-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester. 1H-NMR (400 MHz, CDCl3) δ: 4.39 (q, J=7.1 Hz, 2H), 4.03 (s, 3H), 3.83 (s, 3H), 1.42 (t, J=7.2 Hz, 3H), 1.34 (s, 9H).
Workup
- stirringthe resulting mixture was stirred at room temperature for 12 h
- customThe solvent was removed under reduced pressure
- dissolutionthe resulting residue was dissolved in dry EtOH (2 mL)
- stirringthe resulting mixture was stirred at 80° C. for 8 h
- customThe solvent was removed under reduced pressure
- customthe resulting residue was chromatographed on a 24-g SiO2 pre-packed column
- washeluting with 0:1-3:7 EtOAc/hexanes
Sources & evidence
- ORD record
- ord-80a778eefe554284b542a2462b94bd05
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08680098B2
Linked notes
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