Reaktion #7804
ord-10019520ef6f48319b08b25838da63f4
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)
- 4TemperaturThe reaction was then warmed to rt for 1 h
- 5Sonstigethe precipitate was removed by filtration
- 6EinengenThe filtrate was concentrated
- 7Sonstigedried in vacuo
- 8workup.DISSOLUTIONthe dark brown solid residue was dissolved in toluene (20 mL)
- 9TemperaturThe reaction was refluxed overnight
- 10Temperaturcooled to rt
- 11WaschenThe organic 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 SOCl2 (15 mL) dropwise. The reaction was refluxed for 30 min, cooled to rt and the excess of SOCl2 was removed in vacuo. The oily acid chloride was dissolved in THF (15 mL) and the 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 reaction was then warmed to rt for 1 h and the precipitate was removed by filtration. The filtrate was concentrated and dried in vacuo and the 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 to rt and dissolved in EtOAc (500 mL). The organic 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)+.