Methanol → HCID 21250760, compound

HRID 1532118Notes

Reaction equation

HRID 1532118 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. C6H8ClN3O3requires 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-88a382661cb44761a76831b0519df316
Source dataset
uspto-grants-2001_03
Patent number
US06200980B1

Reaction notes

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