Hydrochloric Acid → Methyl 5-amino-2-hydroxybenzoate

HRID 1027737Notes

Reaction equation

HRID 1027737 reaction equation
Cl.[NH2:2][C:3]1[CH:4]=[CH:5][C:6]([OH:12])=[C:7]([CH:11]=1)[C:8]([OH:10])=[O:9].[CH3:13]O>>[NH2:2][C:3]1[CH:4]=[CH:5][C:6]([OH:12])=[C:7]([CH:11]=1)[C:8]([O:10][CH3:13])=[O:9]

Participants

4

Procedure

To a solution of saturated HCl in CH3OH (20 mL) at RT was slowly added 5-amino-2-hydroxybenzoic acid (2 g, 13.06 mmol). The resulting mixture was stirred at (RT, 16 h) and then heated (reflux, 24 h). The mixture was cooled and the solvent was removed under reduced pressure. The residue was diluted with EtOAc (50 mL) and washed with saturated aqueous NaHCO3. The organic solution was dried over MgSO4, filtered, concentrated under reduced pressure to afford methyl 5-amino-2-hydroxybenzoate as a pale yellow solid (1.72 g, 78.5%). Mass calculated for C8H9NO3=167.16. found: [M+H]+=168.2.

Workup

  1. customat RT
  2. temperatureheated
  3. temperature(reflux, 24 h)
  4. temperatureThe mixture was cooled
  5. customthe solvent was removed under reduced pressure
  6. additionThe residue was diluted with EtOAc (50 mL)
  7. washwashed with saturated aqueous NaHCO3
  8. dry with materialThe organic solution was dried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-1ed8f010f69c45f6a41eb20a357edab5
Source dataset
uspto-grants-2014_05
Patent number
US08735378B2

Reaction notes

Loading…