تفاعل #78906

ord-f4b44a2492fb47cf93b9bdf88797f5df

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA sealed pressure flask, flushed with N2
  2. 2
    workup.ADDITIONcontaining
  3. 3
    درجة الحرارةheated at 90° C. for 18 hours
  4. 4
    ترشيحThe reaction mixture was filtered through celite
  5. 5
    غسيلthe celite was washed with EtOAc (3×30 mL) until the filtrate
  6. 6
    تجفيفThe combined organics were dried over Na2SO4
  7. 7
    تركيزconcentrated on a rotary evaporator
  8. 8
    أخرىThe desired product was purified by silica gel flash chromatography

الإجراء التجريبي

A sealed pressure flask, flushed with N2, containing a mixture of 4-bromo-benzoic acid ethyl ester (2a) (5 g, 0.0218 mol), diethyl phosphite (3.093 mL, 0.024 mol), NMM (2.88 mL, 0.0262 mmol) and Pd(PPh3)4 (2.017 g, 0.00175 mol) in acetonitrile (20 mL) was stirred at ambient temperature for 5-10 min, then heated at 90° C. for 18 hours. The reaction mixture was filtered through celite, and the celite was washed with EtOAc (3×30 mL) until the filtrate showed little or no evidence of product by HPLC. The combined organics were dried over Na2SO4 and concentrated on a rotary evaporator. The desired product was purified by silica gel flash chromatography to give a pale yellow oil (4.24 g). 1H NMR (300 MHz, CDCl3) δ (ppm)) 1.36 (m, 6H), 1.42 (t, J=7 Hz, 3H), 4.16 (m, 4H), 4.42 (q, J=7 Hz, 2H), 7.93 (m, 2H), 8.15 (m, 2H). 31P NMR (121 MHz, CDCl3) δ17.63.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06713462B2uspto-grants-2004_03