Reacción #69565

ord-482d535ef50f4cb0ae074e5269c7e9b0

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONA 3-liter recovery flask was charged with the
  2. 2
    workup.ADDITIONAfter the end of addition
  3. 3
    workup.STIRRINGthe solution was stirred at 50° C. for 7 hours
  4. 4
    Otrothe aqueous phase was removed by separation
  5. 5
    workup.ADDITIONacetone 1 liter was added for extraction
  6. 6
    FiltraciónThe solid was collected by filtration
  7. 7
    Otrodried under reduced pressure

Procedimiento

A 3-liter recovery flask was charged with the above synthesized 7,7′-dibromo-3,3′,5,5′-tetramethyl-1,1′-biadamantane 48.4 g (100 mmol), 1,3-dibromo benzene 1180 g (500 mmol), and a stirrer. While stirring under a nitrogen flow at room temperature, aluminum bromide (III) 26.7 g (100 mmol) was added little by little. After the end of addition, the solution was stirred at 50° C. for 7 hours. The reaction solution was charged into a 1 mol/liter hydrochloric acid solution 2 liter, the aqueous phase was removed by separation, then acetone 1 liter was added for extraction. The solid was collected by filtration and dried under reduced pressure to obtain 7,7′-bis(3,5-dibromophenyl)-3,3′,5,5′-tetramethyl-1,1′-biadamantane (90.0 mmol; yield 90.0%) 71.5 g.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08530596B2uspto-grants-2013_09