Reacción #46030
ord-b88aec028ab3465a9637eaaccef53927
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGby stirring at ambient temperature for 4 hours
- 2OtroAfter terminating
- 3Otrothe reaction
- 4Extracciónthe aqueous layer was extracted with toluene, which
- 5workup.ADDITIONwas added to the organic layer
- 6Lavadothe organic layer was washed with a saturated salt solution
- 7Secadodried over anhydrous magnesium sulfate
- 8workup.DISTILLATIONThe solvent was distilled off
Procedimiento
Under a nitrogen atmosphere, 1.52 g of sodium hydride was added to 9.45 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)phenol (5) dissolved in 60 mL of THF cooling with iced water, and the mixture was stirred at ambient temperature for 30 minutes. 3.07 g of chloromethyl methyl ether was added to the solution under cooling with iced water, followed by stirring at ambient temperature for 4 hours. After terminating the reaction by pouring water into the reaction solution, the aqueous layer was extracted with toluene, which was added to the organic layer, and the organic layer was washed with a saturated salt solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 11.6 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)-1-methoxymethoxybenzene (6).