Reaktion #7802
ord-bde3b58972f64cb4a1179033e865bdef
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe reaction was refluxed for 30 min
- 2SonstigeThe excess of SOCl2 was removed in vacuo
- 3workup.DISSOLUTIONthe oily acid chloride was dissolved in THF (15 mL)
- 4SonstigeThe resulting reaction mixture
- 5Sonstigethe resulting precipitate was removed by filtration
- 6EinengenThe filtrate was concentrated
- 7Sonstigedried under vacuum
- 8workup.DISSOLUTIONThe resulting dark brown solid residue was dissolved in toluene (20 mL)
- 9TemperaturThe reaction was refluxed overnight
- 10Temperaturcooled at rt
- 11WaschenThe EtOAc solution was washed with brine (3×50 mL)
- 12Trocknendried (MgSO4)
- 13Filtrationfiltered
- 14Einengenconcentrated in vacuo
- 15SonstigeThe residue was recrystallized in EtOAc
Vorschrift
To a 100 mL round-bottom flask with 3-hydroxy-4-methylbenzoic acid (2.5 g, 16.4 mmol), was added dropwise SOCl2 (15 mL). The reaction was refluxed for 30 min and cooled to rt. The excess of SOCl2 was removed in vacuo and the oily acid chloride was dissolved in THF (15 mL). This resulting solution was added dropwise to a mixture of 2-aminophenol (1.8 g, 16.4 mmol), triethylamine (1.7 g, 16.4 mmol) and THF (30 mL) at 0° C. The resulting reaction mixture was then brought to rt for 30 min and the resulting precipitate was removed by filtration. The filtrate was concentrated and dried under vacuum. The resulting dark brown solid residue was dissolved in toluene (20 mL) and p-toluenesulfonic acid (15.6 g, 82 mmol) was added. The reaction was refluxed overnight, cooled at rt and EtOAc (500 mL) was added. The EtOAc solution was washed with brine (3×50 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was recrystallized in EtOAc to afford 5-(1,3-benzoxazol-2-yl)-2-methylphenol as a light yellow solid. MS (ESI) 226 (M+H)+.