Reaction #338898
ord-aa19830375ae498f861f99381caea4dc
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1workup.ADDITIONwere charged
- 2OtherAfter reaction solution
- 3Otherreached room temperature
- 4OtherAn aqueous layer was separated
- 5Otherremoved
- 6OtherThen, solvent was removed from the reaction solution under reduced pressure
- 7OtherSolid thus obtained
- 8Otherwas 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%).