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

HRID 403263
Notes
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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]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 31541781-(Difluoromethyl)-1H-pyrazole-3-carboxylic acid

Product 1

HCID 57497167Methyl 1-(difluoromethyl)-1H-pyrazole-3-carboxylate

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
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08748418B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes