Methanol → Methyl 1-(difluoromethyl)-1H-pyrazole-3-carboxylate

HRID 403263Notes

Reaction equation

HRID 403263 reaction equation
[F:1][CH:2]([F:11])[N:3]1[CH:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[N:4]1.S(=O)(=O)(O)O.[CH3:17]O>>[CH3:17][O:9][C:8]([C:5]1[CH:6]=[CH:7][N:3]([CH:2]([F:1])[F:11])[N:4]=1)=[O:10]

Participants

4

Conditions

Temperature
23 °C

Procedure

A solution of 1-difluoromethyl-1H-pyrazole-3-carboxylic acid (CAS [925179-02-8]) (500 mg, 3.1 mmole) in methanol (18 ml) was cooled to 0° C. and treated with sulfuric acid (98%, 0.2 ml, 3.1 mmol). The mixture was heated to reflux for 2 hours, cooled to 23° C. and concentrated at reduced pressure. The residue was partitioned between AcOEt and water, the organic layer was washed with water until the water phase showed a neutral pH, dried and evaporated to give the title compound (535 mg) as a colorless liquid which was used without further purification. MS: m/z=177.1 [M+H]+.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 2 hours
  3. concentrationconcentrated at reduced pressure
  4. customThe residue was partitioned between AcOEt and water
  5. washthe organic layer was washed with water until the water phase
  6. customdried
  7. customevaporated

Sources & evidence

ORD record
ord-df414fa38c48451dba5d59009f63c3ca
Source dataset
uspto-grants-2014_06
Patent number
US08748418B2

Reaction notes

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