Réaction #1951060
ord-e4df4db5f71347d6b5a9f468b3b20741
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températureheated
- 2Températureto cool to ambient temperature
- 3LavageThe solution was washed with saturated sodium bicarbonate (350 mL)
- 4SéchageThe organic phase was dried with magnesium sulfate
- 5Filtrationfiltered
- 6Concentrationconcentrated by rotary evaporation
Mode opératoire
Bromomethyl-cyclopropane (26.00 g, 0.193 mol) was added to triisopropyl phosphite (35.9 mL, 0.30 mol) at ambient temperature, under a nitrogen atmosphere. The resulting solution was stirred and heated at reflux (144° C. bath temperature) 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 rotary evaporation and then under high vacuum to yield 39.96 g of cyclopropylmethyl-phosphonic acid diisopropyl ester (0.182 mol, 94% yield) as a colorless oil. 1H NMR (400 MHz, DMSO) δ 4.63-4.54 (m, 2H); 1.67-1.60 (d of d, 2H) 1.27-1.24 (d of d, 12H); 0.85-0.75 (m, 1H); 0.52-0.46 (m, 2H); 0.21-0.16 (m, 2H); ESMS (m/z): M+1)+ found, 221; (M+23)+ found, 243.