Sodium Hydroxide → 4-(2-Pyridyloxy)-2-phenylbenzoic acid

HRID 383078Notes

Reaction equation

HRID 383078 reaction equation
C[O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=2)=[CH:6][C:5]=1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[OH-].[Na+]>CO.O>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[O:10][C:7]1[CH:8]=[CH:9][C:4]([C:3]([OH:23])=[O:2])=[C:5]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:6]=1

Participants

5

Procedure

A solution of the resultant ester from Example 6B (1.0 equivalent) in aqueous methanol is treated with NaOH (2.0 equivalents) and stirred until the reaction is deemed complete by TLC analysis. The mixture is acidified, diluted with water, and extracted into ethyl acetate which is dried and evaporated. Chromatography on silica gel provides the title product.

Workup

  1. extractionextracted into ethyl acetate which
  2. customis dried
  3. customevaporated

Sources & evidence

ORD record
ord-77936c1c077442e0a2392085d53e0c78
Source dataset
uspto-grants-2001_10
Patent number
US06310095B1

Reaction notes

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