Reacción #2286288
ord-441ca798fc574393bf52db6afd7d43ca
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1ConcentraciónAt this time, the reaction mixture was concentrated under vacuum
- 2workup.ADDITIONThe resulting solid was diluted with water and ethyl acetate
- 3workup.ADDITIONThe water layer was acidified by the addition of a 1N aqueous hydrochloric acid solution
- 4Extracciónwas extracted with ethyl acetate
- 5LavadoThe organic layers were washed with a saturated aqueous sodium chloride solution
- 6Secadodried with magnesium sulfate
- 7Filtraciónfiltered
- 8Concentraciónconcentrated under vacuum
Procedimiento
A solution of [3-chloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-5-methyl-phenyl]-acetic acid methyl ester (8b) (1.1 g, 2.97 mmol) in methanol (30 mL) at room temperature was treated dropwise with a 1N aqueous sodium hydroxide solution (5.9 mL, 5.9 mmol). The reaction was stirred at room temperature for 4 d. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water and ethyl acetate. The ethyl acetate layer was discarded. The water layer was acidified by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate. The organic layers were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum to afford [3-chloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-5-methyl-phenyl]-acetic acid (9b) (1.05 g, 100%) as a white solid. This material was used without further purification; EI(+)-HRMS m/z calcd for C16H16Cl2N2O3 (M+) 355.0611, found 355.0610. Molecular Weight=355.2235; Exact Mass=354.0538