Sodium Hydroxide → 3,5-Dimethoxy-2-methylbenzoic acid

HRID 1384332Notes

Reaction equation

HRID 1384332 reaction equation
[CH3:1][O:2][C:3]1[C:4]([CH3:15])=[C:5]([CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1)[C:6]([O:8]C)=[O:7].[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[C:4]([CH3:15])=[C:5]([CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1)[C:6]([OH:8])=[O:7]

Participants

4

Procedure

Solid methyl 3,5-dimethoxy-2-methylbenzoate (5.83 g, J. C. S. Perkin I, 1973, 2853.) was dissolved in methanol (80 ml). A solution of aqueous sodium hydroxide (10%, 80 ml) was added and the solution stirred at room temperature for 1 hour. The reaction was then concentrated under reduced pressure to approximately half of the original volume before adding aqueous hydrochloric acid (200 ml). The white precipitate that formed was extracted with ethyl acetate (2×250 ml). The combined extracts were dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure to give the sub-title compound as a colourless solid (5.41 g).

Workup

  1. concentrationThe reaction was then concentrated under reduced pressure to approximately half of the original volume
  2. additionbefore adding aqueous hydrochloric acid (200 ml)
  3. customThe white precipitate that formed
  4. extractionwas extracted with ethyl acetate (2×250 ml)
  5. dry with materialThe combined extracts were dried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-4e8ba86960b2481cac3204b35734007a
Source dataset
uspto-grants-2001_07
Patent number
US06258838B1

Reaction notes

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