تفاعل #92813

ord-b1a99e4574d64a38801f876484d345f0

معادلة التفاعل

c1ccc2c(c1)N=c1c-2ccc2c1=Nc1ccccc1-2
Indolo[2,3-a]carbazole
Brc1cccc(-c2ccc(-c3ccccc3)cc2)c1
3-bromo-p-terphenyl
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium orthophosphate
c1ccc(-c2ccc(-c3cccc(-n4c5ccccc5c5ccc6c7ccccc7[nH]c6c54)c3)cc2)cc1
N-(1,1′:4′,1″-terphenyl-3-yl)indolo[2,3-a]carbazole
المردود 67.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    درجة الحرارةto reflux for 16 h
  3. 3
    أخرىAfter the completion of reaction
  4. 4
    أخرىthe reaction was quenched with water
  5. 5
    استخلاصThe reaction mixture was then extracted
  6. 6
    تجفيفand the organic layer was dried over anhydrous sodium sulfate
  7. 7
    أخرىevaporated to dryness under vacuum

الإجراء التجريبي

Indolo[2,3-a]carbazole (9.8 g) was dissolved in 150 ml of dry toluene under nitrogen. 12.9 g of 3-bromo-p-terphenyl, 0.65 g of tris(dibenzylideneacetone) dipalladium, 0.46 g of tri-t-butylphosphine and 40.3 g of potassium orthophosphate were added and heated to reflux for 16 h. After the completion of reaction, the reaction was quenched with water. The reaction mixture was then extracted using ethyl acetate; and the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness under vacuum. Subsequent silica gel column chromatography using ethyl acetate/hexane (1:9) as eluent, yielded 12.6 g of N-(1,1′:4′,1″-terphenyl-3-yl)indolo[2,3-a]carbazole.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09450192B2uspto-grants-2016_09