Reaktion #5394

ord-55908127f3db4593a4b9cdbbe3effaaf

Reaktionsgleichung

COc1cccc(-c2cc(OC)ccc2C(=O)O)c1
2-carboxy-5,5'-dimethoxybiphenyl
COc1ccc2c(c1)-c1cc(OC)ccc1C2=O
3,6-dimethoxy-9-fluorenone
Ausbeute 96.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto obtain a dark brown solution
  2. 2
    Temperaturheated at 40°-50° C. for 5 hours
  3. 3
    Temperaturcooled to room temperature
  4. 4
    workup.ADDITIONThe reaction mixture was then poured
  5. 5
    Sonstigeonto crushed ice
  6. 6
    Sonstigeto form a yellow colored precipitate which
  7. 7
    Filtrationwas collected by filtration
  8. 8
    WaschenThe precipitate was washed with large amounts of water
  9. 9
    Sonstigeair dried

Vorschrift

7.5 g of 2-carboxy-5,5'-dimethoxybiphenyl was dissolved in 75 mL of methanesulfonic acid to obtain a dark brown solution. The solution was stirred at room temperature for one hour, heated at 40°-50° C. for 5 hours and then cooled to room temperature. The reaction mixture was then poured onto crushed ice to form a yellow colored precipitate which was collected by filtration. The precipitate was washed with large amounts of water and then air dried to yield 6.7 g of crude 3,6-dimethoxy-9-fluorenone. Recrystallization from ethanol followed by column chromatography on silica gel using methylene chloride as the eluent yielded pure 3,6-dimethoxy-9-fluorenone. The structure was confirmed by NMR and mass spectroscopy.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244771uspto-grants-1993_09