Methanol → HCID 21250760, compound
Reaction equation
Br[CH2:2][C:3]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([Cl:11])[N:5]([CH3:12])[N:4]=1.[CH3:13][OH:14]>[N+]([O-])([O-])=O.[Ag+]>[Cl:11][C:6]1[N:5]([CH3:12])[N:4]=[C:3]([CH2:2][O:14][CH3:13])[C:7]=1[N+:8]([O-:10])=[O:9]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-bromomethyl-5-chloro-1-methyl-4-nitropyrazole (5.0 g, 19.6 mmol) in methanol (50 ml) was treated with silver nitrate (5.75 g, 33.8 mmol) and the mixture heated under reflux for 2 hours. The cooled reaction mixture was filtered and the filtrate evaporated under vacuum. The residue was partitioned between ethyl acetate (100 ml) and water (50 ml ) and the aqueous phase extracted with a further quantity of ethyl acetate (50 ml). The organic extracts were combined, dried (MgSO4) and evaporated under vacuum. Chromatography on silica gel, eluting with a 97:3 mixture of dichloromethane and methanol, gave the title pyrazole as a white solid (1.6 g, 40%), m.p. 59°-63° C. Found: C,34.65; H, 3.83; N,20.05. C6H8ClN3O3 recreates C,35.05; H, 3.92; N, 20.44%.
Workup
- temperaturethe mixture heated
- temperatureunder reflux for 2 hours
- customThe cooled reaction mixture
- filtrationwas filtered
- customthe filtrate evaporated under vacuum
- customThe residue was partitioned between ethyl acetate (100 ml) and water (50 ml )
- extractionthe aqueous phase extracted with a further quantity of ethyl acetate (50 ml)
- dry with materialdried (MgSO4)
- customevaporated under vacuum
- washChromatography on silica gel, eluting with a 97:3 mixture of dichloromethane and methanol
Sources & evidence
- ORD record
- ord-b95555cdf3ce4df5ab239c7f0e97cfff
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719283
Reaction notes
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