Potassium Hydroxide → 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetic acid

HRID 56497Notes

Reaction equation

HRID 56497 reaction equation
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([CH:12]([O:17][CH3:18])[C:13]([O:15]C)=[O:14])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1.[OH-].[K+]>CO>[N:1]1([C:6]2[CH:7]=[CH:8][C:9]([CH:12]([O:17][CH3:18])[C:13]([OH:15])=[O:14])=[CH:10][CH:11]=2)[CH:5]=[CH:4][CH:3]=[N:2]1

Participants

4

Procedure

To a stirred solution of methyl 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetate (0.204 g, 0.83 mmol) in dry MeOH (5 mL) under argon was added a solution of KOH in MeOH (1.6 mL of a 0.5 M solution, 8.3 mmol) and the reaction was heated to reflux for 5 hours. The reaction mixture was cooled to room temperature and the volatiles were removed under reduced pressure. The residue was diluted with saturated aqueous NH4Cl and extracted with EtOAc. Additional EtOAc was then used to extract the aqueous phase as the pH was adjusted from ˜8 to ˜2 using concentrated HCl. The combined organics were dried over Na2SO4, filtered, and the solvents removed under reduced pressure to yield 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetic acid (0.18 g, 95%) which was used without further purification.

Workup

  1. temperaturewas heated
  2. temperatureto reflux for 5 hours
  3. customthe volatiles were removed under reduced pressure
  4. additionThe residue was diluted with saturated aqueous NH4Cl
  5. extractionextracted with EtOAc
  6. extractionto extract the aqueous phase as the pH
  7. dry with materialThe combined organics were dried over Na2SO4
  8. filtrationfiltered
  9. customthe solvents removed under reduced pressure

Sources & evidence

ORD record
ord-7675d9d5f9c94ee09f766a8e3bf668f7
Source dataset
uspto-grants-2016_09
Patent number
US09434707B2

Reaction notes

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