Réaction #1951060

ord-e4df4db5f71347d6b5a9f468b3b20741

Équation de réaction

BrCC1CC1
Bromomethyl-cyclopropane
CC(C)OP(OC(C)C)OC(C)C
triisopropyl phosphite
CC(C)OP(=O)(CC1CC1)OC(C)C
cyclopropylmethyl-phosphonic acid diisopropyl ester
Rendement 94.3%

Conditions de réaction

Température
144°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureheated
  2. 2
    Températureto cool to ambient temperature
  3. 3
    LavageThe solution was washed with saturated sodium bicarbonate (350 mL)
  4. 4
    SéchageThe organic phase was dried with magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Concentrationconcentrated 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.

Source

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