Reaktion #1605771

ord-2248bc55a7674b14921a08ad02a489ba

Reaktionsgleichung

Cc1ccc(C(=O)O)c(O)c1
2-hydroxy-4-methylbenzoic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
[K+].[OH-]
KOH
Cl
HCl
COc1cc(C)ccc1C(=O)O
2-methoxy-4-methylbenzoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture heated
  2. 2
    Temperaturat reflux for 48 hrs
  3. 3
    Filtrationwas filtered
  4. 4
    Sonstigethe filtrate was evaporated
  5. 5
    Sonstigeto give the crude methyl 2-methoxy-4-methylbenzoate
  6. 6
    Temperaturthe solution heated
  7. 7
    Temperaturat reflux 48 hrs
  8. 8
    TemperaturAfter cooling the reaction mixture
  9. 9
    Extraktionextracted with ethyl acteate
  10. 10
    WaschenThe organic layer was washed with brine
  11. 11
    Trocknendried over MgSO4
  12. 12
    Filtrationfiltered
  13. 13
    Sonstigeevaporated
  14. 14
    SonstigeThe residue was triturated with Ethyl acetate/Hexane

Vorschrift

To a solution of 2-hydroxy-4-methylbenzoic acid (25 g, 0.164 mol) in acetone (350 mL) was added K2CO3 (68 g, 0.492 mmol) followed by MeI (41 mL, 0.656 mmol) and the reaction mixture heated at reflux for 48 hrs. After cooling to r.t. the reaction mixture was filtered and the filtrate was evaporated to give the crude methyl 2-methoxy-4-methylbenzoate. KOH (11.3 g, 1.2 eq) was dissolved in MeOH (300 mL) and the crude ester was added to the mixture and the solution heated at reflux 48 hrs. After cooling the reaction mixture was acidified with aq. HCl (1N) and extracted with ethyl acteate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was triturated with Ethyl acetate/Hexane to give 20 g of 2-methoxy-4-methylbenzoic acid as a cream white solid (85% yield)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09072313B2uspto-grants-2015_07