Reaktion #1605771
ord-2248bc55a7674b14921a08ad02a489ba
Reaktionsgleichung
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturthe reaction mixture heated
- 2Temperaturat reflux for 48 hrs
- 3Filtrationwas filtered
- 4Sonstigethe filtrate was evaporated
- 5Sonstigeto give the crude methyl 2-methoxy-4-methylbenzoate
- 6Temperaturthe solution heated
- 7Temperaturat reflux 48 hrs
- 8TemperaturAfter cooling the reaction mixture
- 9Extraktionextracted with ethyl acteate
- 10WaschenThe organic layer was washed with brine
- 11Trocknendried over MgSO4
- 12Filtrationfiltered
- 13Sonstigeevaporated
- 14SonstigeThe 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)