تفاعل #1951067

ord-0e3cd0923ddf44ee93452bf59e22c56d

معادلة التفاعل

Fc1ccc(Br)cc1
4-Bromo-fluorobenzene
CCOP([O-])OCC
diethyl phosphite
CCN(CC)CC
triethylamine
CCOP(=O)(OCC)c1ccc(F)cc1
4-fluorophenyl-phosphonic acid diethyl ester
المردود 94.0%

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting solution was degassed with nitrogen
  2. 2
    درجة الحرارةto cool to ambient temperature
  3. 3
    غسيلThe solution was washed with saturated sodium bicarbonate (350 mL)
  4. 4
    workup.DISTILLATIONThe crude product was purified by vacuum distillation (ca. 98° C., 0.6 Torr)

الإجراء التجريبي

4-Bromo-fluorobenzene (10.95 g, 62.57 mmol) was added to diethyl phosphite (8.86 mL, 68.8 mmol) at ambient temperature, followed by the addition of triethylamine (9.6 mL, 68.8 mmol). The resulting solution was degassed with nitrogen followed by the addition of tetrakis(triphenylphosphine)-palladium (3.0 g, 2.6 mmol). The resulting mixture was heated at 90° C. overnight. The reaction mixture was allowed to cool to ambient temperature and then ethyl acetate (350 mL) was added. The solution was washed with saturated sodium bicarbonate (350 mL) and then with saturated brine (2×350 mL). The crude product was purified by vacuum distillation (ca. 98° C., 0.6 Torr) to yield 8.956 g of 4-fluorophenyl-phosphonic acid diethyl ester (38.6 mmol, 94% yield) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.88-7.80 (m, 2H); 7.20-7.14 (m 2H); 4.22-4.04 (m, 4H); 1.36-1.32 (t, 6H); ESMS (m/z): M+1)+ found, 233.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07625880B2uspto-grants-2009_12