Lithium Hydroxide → 2-Methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic Acid

HRID 1635882Notes

Reaction equation

HRID 1635882 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]([N:13]2[CH:17]=[CH:16][C:15]([CH3:18])=[N:14]2)[CH:10]=[CH:9][C:4]=1[C:5]([O:7]C)=[O:6].[OH-].[Li+]>O1CCCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]([N:13]2[CH:17]=[CH:16][C:15]([CH3:18])=[N:14]2)[CH:10]=[CH:9][C:4]=1[C:5]([OH:7])=[O:6]

Participants

4

Reactant 2

HCID 3939Lithium HydroxideHCID 544211052-Methoxy4-(3-methyl-pyrazol-1-yl)-benzoic acid, methyl ester

Product 1

HCID 226054612-Methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic Acid

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A solution of 2-methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic acid methyl ester (0.5 g) from Example 105 in tetrahydrofuran (2.5 ml) was treated with 1 N lithium hydroxide (2.13 ml) at room temperature. After 14 hours the solvent was removed in vacuo and the title compound precipitated by the addition at 0° C. of 1N hydrochloric acid. After drying under vacuum 0.42 g of the title compound was obtained as a solid. MS, m/z: 232 (M)+.

Workup

  1. customAfter 14 hours the solvent was removed in vacuo
  2. customthe title compound precipitated by the addition at 0° C. of 1N hydrochloric acid
  3. dry with materialAfter drying under vacuum 0.42 g of the title compound
  4. customwas obtained as a solid

Sources & evidence

ORD record
ord-bcaf02d28ec04c93a83aa3ecfd81e942
Source dataset
uspto-grants-2003_01
Patent number
US06511974B1

Reaction notes

Loading…