Reacción #347900

ord-266f65c38c6d41cfbdb52275a0f7a04a

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONthe reaction mixture was poured
  2. 2
    workup.STIRRINGwhile stirring
  3. 3
    Otrothe tetrahydrofuran was removed under reduced pressure
  4. 4
    LavadoThe resulting alkaline aqueous solution was washed with methylene chloride
  5. 5
    Filtraciónthe precipitated crystals were collected by filtration
  6. 6
    Otrodried

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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05530021uspto-grants-1996_06