Reaktion #9799

ord-2b9cd45206bd483889c44f0a2aa70c02

Lösungsmittel

Reaktionsbedingungen

Temperatur
-30°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe reaction was stirred
  2. 2
    Temperaturwarmed to RT over 30 min
  3. 3
    SonstigeThe volatiles were removed under N2
  4. 4
    Sonstigepurge
  5. 5
    workup.DISSOLUTIONthe residue was redissolved in 3:1 THF/NMP (11 mL)
  6. 6
    Temperaturthe reaction was heated to 100° C. for 2 h
  7. 7
    TemperaturThe reaction was cooled to RT
  8. 8
    Sonstigethe THF was removed
  9. 9
    workup.ADDITIONThe residue was diluted with CH2Cl2
  10. 10
    Waschenwashed with 1 M HCl
  11. 11
    Trocknendried over Na2SO4
  12. 12
    SonstigeThe crude material was purified by flash chromatography

Vorschrift

A solution of 9-bromoanthracene (0.67 g, 2.6 mmol, 1.2 eq) in dry Et2O (13 mL) under N2 was cooled to −30° C. and nBuli (1.6 M in hexane, 1.6 mL, 2.6 mmol, 1.2 eq) was added dropwise. The solution was stirred for 20 min. at −30° C. followed by dropwise addition of ZnCl2 (0.50 M in THF, 5.2 mL, 2.6 mmol, 1.2 eq). The reaction was stirred and warmed to RT over 30 min. The volatiles were removed under N2 purge and the residue was redissolved in 3:1 THF/NMP (11 mL). The MOM-protected bromophenol (2.2 mmol, 1.0 eq) and Pd(PtBu3)2 (22 mg, 44 μmol, 4 mol %) were added and the reaction was heated to 100° C. for 2 h. The reaction was cooled to RT and the THF was removed. The residue was diluted with CH2Cl2, washed with 1 M HCl, and dried over Na2SO4. The crude material was purified by flash chromatography.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091292B2uspto-grants-2006_08