Réaction #1951056
ord-8cabd193a6274e308e46071ebbde90ad
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Autreat 90° C.
- 2Autreovernight
- 3Températureto cool to ambient temperature
- 4LavageThe solution was washed with saturated sodium bicarbonate (350 mL)
- 5SéchageThe organic phase was dried with magnesium sulfate
- 6Filtrationfiltered
- 7Concentrationconcentrated by rotatry evaporation
- 8AutreThe 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.