Potassium Hydroxide → 4-(5-Fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-trifluoromethyl-valeric acid

HRID 1266421Notes

Reaction equation

HRID 1266421 reaction equation
C([O:3][C:4](=[O:24])[C:5]([OH:23])([C:19]([F:22])([F:21])[F:20])[CH2:6][C:7]([C:10]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=1[O:17][CH3:18])([CH3:9])[CH3:8])C.[OH-].[K+]>CO>[F:16][C:14]1[CH:13]=[CH:12][C:11]([O:17][CH3:18])=[C:10]([C:7]([CH3:8])([CH3:9])[CH2:6][C:5]([OH:23])([C:19]([F:22])([F:21])[F:20])[C:4]([OH:24])=[O:3])[CH:15]=1

Participants

4

Procedure

1.9 g of 4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-trifluoromethyl-valeric acid ethyl ester is refluxed with 40 ml of potassium hydroxide in methanol (10%) for 2 hours. After the solvent is concentrated by evaporation in a vacuum, water is added, it is extracted with hexane, and the separated water phase is acidified with 6N hydrochloric acid. After extraction with ethyl acetate, the ethyl acetate phase is washed with water, dried (Na2SO4) and concentrated by evaporation. The residue is crystallized from hexane. 1.55 g of 4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-trifluoromethyl-valeric acid, melting point 102-104° C., is obtained.

Workup

  1. concentrationAfter the solvent is concentrated by evaporation in a vacuum, water
  2. additionis added
  3. extractionit is extracted with hexane
  4. extractionAfter extraction with ethyl acetate
  5. washthe ethyl acetate phase is washed with water
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated by evaporation
  8. customThe residue is crystallized from hexane

Sources & evidence

ORD record
ord-834ad23ebba3469a8ee8b031ea03a4de
Source dataset
uspto-grants-2003_04
Patent number
US06548534B2

Reaction notes

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