تفاعل #44311

ord-cde1b627deb84233936c4eac8d7f92d5

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe resulting mixture was heated
  2. 2
    درجة الحرارةat reflux under nitrogen for 10 days
  3. 3
    ترشيحThe reaction mixture was filtered
  4. 4
    أخرىto remove the sodium salts
  5. 5
    تركيزThe filtrate was concentrated to dryness
  6. 6
    أخرىto give the crude product as a pale brown solid
  7. 7
    أخرىThe crude product was purified first by chromatography on silica
  8. 8
    أخرىfollowed by recrystallisation from toluene
  9. 9
    أخرىwas then sublimed at 280-281° C. at 10−6 mm Hg

الإجراء التجريبي

Tri-tert-butylphosphine (304 mg, 1.50 mmol) in toluene (38 ml) was added under nitrogen to a deoxygenated mixture of carbazole (16.9 g, 0.100 mmol), 4,4′-dibromobiphenyl (15.7 g, 50.4 mmol), sodium tert-butoxide (30.9 g, 321 mmol) and palladium acetate (115 mg, 0.512 mmol) in toluene (50 ml) and the resulting mixture was heated at reflux under nitrogen for 10 days. The reaction mixture was cooled to room temperature and then diluted with more toluene (200 ml). The reaction mixture was filtered to remove the sodium salts. The filtrate was concentrated to dryness to give the crude product as a pale brown solid. The crude product was purified first by chromatography on silica using dichloromethane as the eluent followed by recrystallisation from toluene. The material was then sublimed at 280-281° C. at 10−6 mm Hg to give the product 4,4′-bis(carbazol-9-yl)biphenyl (1) (18.3 g, 75%), as an off-white solid with melting point 280-281° C. (lit. m.p. 281° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07736534B2uspto-grants-2010_06