Hydrochloric Acid → Methyl 5-amino-2-hydroxybenzoate

HRID 1844653Notes

Reaction equation

HRID 1844653 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-5f5cf0f81d254d7da2aaff9baead1f05
Source dataset
uspto-grants-2015_02
Patent number
US08946451B2

Reaction notes

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