Methanol → HCID 21250760, compound

HRID 862907Notes

Reaction equation

HRID 862907 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

4

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

  1. temperaturethe mixture heated
  2. temperatureunder reflux for 2 hours
  3. customThe cooled reaction mixture
  4. filtrationwas filtered
  5. customthe filtrate evaporated under vacuum
  6. customThe residue was partitioned between ethyl acetate (100 ml) and water (50 ml )
  7. extractionthe aqueous phase extracted with a further quantity of ethyl acetate (50 ml)
  8. dry with materialdried (MgSO4)
  9. customevaporated under vacuum
  10. 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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