Reaction #338898

ord-aa19830375ae498f861f99381caea4dc

Solvents

Conditions

Temperature
150°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONwere charged
  2. 2
    OtherAfter reaction solution
  3. 3
    Otherreached room temperature
  4. 4
    OtherAn aqueous layer was separated
  5. 5
    Otherremoved
  6. 6
    OtherThen, solvent was removed from the reaction solution under reduced pressure
  7. 7
    OtherSolid thus obtained
  8. 8
    Otherwas purified by column chromatography

Procedure

In a 500 mL recovery flask, 44.9 g of 2,7-di(1-adamantyl)-fluorenone obtained in the same manner as in Synthesis example 7 (100 mmol), 36.6 g of benzoic acid (300 mmol), 203 mL of Eaton's reagent (7.7 wt % methanesulfonic acid solution of diphosphorus pentoxide) and a stirrer were charged and agitated at 150° C. for 12 hours under a nitrogen atmosphere. After reaction solution reached room temperature, mL of ion-exchange water was added slowly. An aqueous layer was separated and removed therefrom. Then, solvent was removed from the reaction solution under reduced pressure. Solid thus obtained was purified by column chromatography, thus obtaining 54.7 g of 2,7-di(1-adamantyl)-fluorene-9,9-bisbenzoic acid (81 mmol; yield: 81%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07863347B2uspto-grants-2011_01