(4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester → (4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid

HRID 548571Notes

Reaction equation

HRID 548571 reaction equation
C[O:2][C:3](=[O:36])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][C:14]#[C:15][C:16]2[CH:21]=[C:20]([C:22]#[C:23][C:24]3[CH:29]=[CH:28][C:27]([C:30]([F:33])([F:32])[F:31])=[CH:26][CH:25]=3)[CH:19]=[C:18]([Br:34])[CH:17]=2)=[CH:8][C:7]=1[CH3:35]>C(O)C.[OH-].[Na+]>[Br:34][C:18]1[CH:17]=[C:16]([C:15]#[C:14][CH2:13][O:12][C:9]2[CH:10]=[CH:11][C:6]([O:5][CH2:4][C:3]([OH:36])=[O:2])=[C:7]([CH3:35])[CH:8]=2)[CH:21]=[C:20]([C:22]#[C:23][C:24]2[CH:29]=[CH:28][C:27]([C:30]([F:32])([F:33])[F:31])=[CH:26][CH:25]=2)[CH:19]=1

Participants

4

Procedure

A solution of (4-{3-[3-bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester (94 mg, 0.169 mmol) in ethanol (5 ml) and 1N NaOH (0.5 ml) was stirred at 75° C. for 30 min. The reaction mixture was evaporated and the residue dissolved in water (2 ml). Aqueous 1N HCl (0.6 ml) was added and the mixture was extracted with methylene chloride (3×15 ml). The combined organic phases were dried and evaporated to give the title compound in 79 mg (86%) yield.

Workup

  1. customThe reaction mixture was evaporated
  2. dissolutionthe residue dissolved in water (2 ml)
  3. additionAqueous 1N HCl (0.6 ml) was added
  4. extractionthe mixture was extracted with methylene chloride (3×15 ml)
  5. customThe combined organic phases were dried
  6. customevaporated

Sources & evidence

ORD record
ord-c7c46ac3bd344538b62c47b77f5a88c4
Source dataset
uspto-grants-2011_05
Patent number
US07943612B2

Reaction notes

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