Sulfuric Acid → Methyl 5-amino-2-hydroxybenzoate

HRID 2107006Notes

Reaction equation

HRID 2107006 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].S(=O)(=O)(O)O.[OH-].[Na+].[C:19](=O)([O-])O.[Na+]>CO>[OH:11][C:5]1[CH:4]=[CH:3][C:2]([NH2:1])=[CH:10][C:6]=1[C:7]([O:9][CH3:19])=[O:8]

Participants

6

Procedure

5-Amino-2-hydroxybenzoic acid (200 g, 1.31 mole) was suspended in methanol (2 1), concentrated sulphuric acid (120 ml) was slowly added and the reaction mixture was refluxed for 48 hours under nitrogen. Subsequently the reaction mixture was brought to room temperature and neutralized with 33% aqueous sodium hydroxide (120 ml) and 1M aqueous sodium hydrogen carbonate (to neutral reaction). The reaction mixture was extracted with ether (3×400 ml), the ethereal solution was washed with 1M aqueous sodium hydrogen carbonate (2×100 ml) and water (2×100 ml) and dried over anhydrous magnesium sulphate (50 g) and the ether evaporated. The remaining product was recrystallized from hexane, with activated carbon, to give methyl 2-hydroxy-5-aminobenzoate (98.3 g, 45%), m.p. 93°-95° C. Found (Calc. for C8H9NO3) C 57.38 (57.48), H 5.41 (5.39), N 8.38 (8.38).

Workup

  1. temperaturethe reaction mixture was refluxed for 48 hours under nitrogen
  2. extractionThe reaction mixture was extracted with ether (3×400 ml)
  3. washthe ethereal solution was washed with 1M aqueous sodium hydrogen carbonate (2×100 ml) and water (2×100 ml)
  4. dry with materialdried over anhydrous magnesium sulphate (50 g)
  5. customthe ether evaporated
  6. customThe remaining product was recrystallized from hexane, with activated carbon

Sources & evidence

ORD record
ord-409342204767477f9a79d4c0e83fb923
Source dataset
uspto-grants-1990_06
Patent number
US04933330

Reaction notes

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