تفاعل #487554

ord-72c1feda0ee1403b9f48c253ac7bd01f

معادلة التفاعل

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCc1ccc(Br)cc1[N+](=O)[O-]
4-bromo-1-ethyl-2-nitrobenzene
OB(O)c1ccc(Cl)cc1
4-chlorophenylboronic acid
CCc1ccc(-c2ccc(Cl)cc2)cc1[N+](=O)[O-]
4′-chloro-4-ethyl-3-nitrobiphenyl
المردود 104.7%

المذيبات

ظروف التفاعل

درجة الحرارة
20°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةmixture is refluxed for 16 hours
  2. 2
    درجة الحرارةThe reaction mixture is cooled to room temperature
  3. 3
    ترشيحfiltered through diatomaceous earth
  4. 4
    غسيلwashing with 200 ml of ethyl acetate
  5. 5
    workup.ADDITIONThe mixture is poured into a separating funnel
  6. 6
    أخرىthe two phases are separated
  7. 7
    استخلاصThe aqueous phase is extracted with ethyl acetate
  8. 8
    تجفيفdried over anhydrous magnesium sulfate
  9. 9
    ترشيحfiltered
  10. 10
    أخرىthe filtrate is evaporated in vacuo

الإجراء التجريبي

To 4-bromo-1-ethyl-2-nitrobenzene (20.0 g, 0.087 mol) in 150 ml 1,2-dimethoxyethane is added, at room temperature, 4-chlorophenylboronic acid (14.98 g, 0.096 mol) and tetrakis(triphenylphosphine)palladium(0) (2.0 g, 0.00174 mol) and nitrogen gas is bubbled through the mixture. After stirring for 10 minutes at 20° C., a solution of sodium carbonate (73.8 g, 0.696 mol) in water (350 ml) is added and mixture is refluxed for 16 hours. The reaction mixture is cooled to room temperature, filtered through diatomaceous earth, washing with 200 ml of ethyl acetate. The mixture is poured into a separating funnel and the two phases are separated. The aqueous phase is extracted with ethyl acetate. The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated in vacuo to give 4′-chloro-4-ethyl-3-nitrobiphenyl (23.84 g) as a brown oil used without further purification in the next step.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741806B2uspto-grants-2014_06