Réaction #1951056

ord-8cabd193a6274e308e46071ebbde90ad

Équation de réaction

Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
COP(OC)OC
trimethyl phosphite
COP(=O)(Cc1ccc(F)cc1)OC
(4-fluoro-benzyl)-phosphonic acid dimethyl ester
Rendement 67.5%

Conditions de réaction

Température
110°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat 90° C.
  2. 2
    Autreovernight
  3. 3
    Températureto cool to ambient temperature
  4. 4
    LavageThe solution was washed with saturated sodium bicarbonate (350 mL)
  5. 5
    SéchageThe organic phase was dried with magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated by rotatry evaporation
  8. 8
    AutreThe resulting crude product was purified by flash silica chromatrography

Mode opératoire

4-fluorobenzyl bromide (25 mL, 0.20 mol) was added to a stirred solution of trimethyl phosphite (35.9 mL, 0.30 mol) at ambient temperature, under a nitrogen atmosphere. The resulting solution was heated at 110° C. for six hours, and then 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 organic phase was dried with magnesium sulfate, filtered, and concentrated by rotatry evaporation. The resulting crude product was purified by flash silica chromatrography using 0-35% acetonitrile in ethyl acetate as eluant to yield (4-fluoro-benzyl)-phosphonic acid dimethyl ester (29.44 g, 135 mmol, 66% yield) as a colorless oil. 1H NMR (400 MHz, DMSO) δ 7.33-7.28 (m, 2H); 7.17-7.12 (dd, 2H); 3.61-3.58 (d, 6H); 3.31-3.24 (d, 2H); ESMS (m/z): (M+1)+ found, 219.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07625880B2uspto-grants-2009_12