Reacción #347900
ord-266f65c38c6d41cfbdb52275a0f7a04a
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONthe reaction mixture was poured
- 2workup.STIRRINGwhile stirring
- 3Otrothe tetrahydrofuran was removed under reduced pressure
- 4LavadoThe resulting alkaline aqueous solution was washed with methylene chloride
- 5Filtraciónthe precipitated crystals were collected by filtration
- 6Otrodried
Procedimiento
In 300 ml of dry tetrahydrofuran, was dissolved 32.0 g of 6-bromo-5-methyl-1,4-benzodioxane and after cooling the solution to -78° C., 96.7 ml of n-butyl lithium (n-hexane solution)was added dropwise over 20 minutes or more. After stirring at the same temperature for 1.5 hours, the reaction mixture was poured onto crushed dry ice and dry ice was sublimated while stirring. Water was added to the -mixture and the tetrahydrofuran was removed under reduced pressure. The resulting alkaline aqueous solution was washed with methylene chloride and adjusted to pH 3 with a 5% hydrochloric acid, and the precipitated crystals were collected by filtration and dried to obtain 20.9 g of 5-methyl-1,4-benzodioxan-6-carboxylic acid (yield: 77%).