تفاعل #554601

ord-f5ac206fbc5c480bab33cb7f2000af89

معادلة التفاعل

C1COCCO1
dioxane
O=S(=O)(Oc1cccc2c3ccccc3c3ccccc3c12)C(F)(F)F
triphenylenyl trifluoromethanesulfonate
CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C
bis(pinacolato)diboron
CC(=O)[O-].[K+]
potassium acetate
OB(O)c1ccc2c3ccccc3c3ccccc3c2c1
triphenylene-2-boronic acid
المردود 51.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe resultant was refluxed
  2. 2
    درجة الحرارةwhile heating for 8 hours
  3. 3
    استخلاصfollowed by extraction with toluene
  4. 4
    أخرىAn aqueous phase was removed
  5. 5
    غسيلan organic phase was washed with water and saturated brine
  6. 6
    تجفيفdried with magnesium sulfate
  7. 7
    أخرىMagnesium sulfate was removed
  8. 8
    workup.DISTILLATIONthe solvent was distilled under reduced pressure
  9. 9
    أخرىThe resulting residue was purified by means of silica gel column chromatography

الإجراء التجريبي

Under an argon atmosphere, 37.6 g of triphenylenyl trifluoromethanesulfonate, 27.9 g of bis(pinacolato)diboron, 2.45 g of 1,1′-bis(diphenylphosphino)ferrocene palladium (II) dichloride dichloromethane complex, 1.66 g of 1,1′-bis(diphenylphosphino)ferrocene and 29.4 g of potassium acetate were placed in a flask. 600 mL of anhydrous dioxane was added thereto, and the resultant was refluxed with stirring while heating for 8 hours. After cooling to room temperature, 300 mL of water was added to the reaction solution, followed by extraction with toluene. An aqueous phase was removed, and an organic phase was washed with water and saturated brine, and then dried with magnesium sulfate. Magnesium sulfate was removed and the solvent was distilled under reduced pressure. The resulting residue was purified by means of silica gel column chromatography, whereby 14.1 g (yield: 40%) of triphenylene-2-boronic acid picohal ester was obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08623520B2uspto-grants-2014_01