Réaction #42020

ord-c4dbe71e53fe47f5aca8f35e02e13474

Équation de réaction

Cl
hydrochloric-acid
CCCCOP([O-])OCCCC
dibutylphosphite
CC(=O)CC(C)C
methyl isobutyl ketone
CCCCOP(=O)(OCCCC)C(C)(O)CC(C)C
dibutyl(1-hydroxy-1,3-dimethylbutyl)phosphonate
Rendement 92.3%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreInto a two-liter four-necked flask provided with a stirrer
  2. 2
    workup.ADDITIONmixed solution at 25° C.
  3. 3
    workup.ADDITIONThe resulting mixed solution
  4. 4
    workup.STIRRINGwas further stirred for 1 hour at the same temperature (25° C.)
  5. 5
    Autrethe reaction
  6. 6
    LavageThereafter, the mixed solution was washed
  7. 7
    Autreto remove the low-boiling point portions
  8. 8
    Autreas in (synthesis of raw material 2) of Example 1
  9. 9
    Autrethus, the triethylamine and the magnesium chloride was removed from the mixed solution

Mode opératoire

Into a two-liter four-necked flask provided with a stirrer, a thermometer, dropping device, a hydrochloric-acid-recovering device and a condenser, 213.4 g (1.1 moles) of dibutylphosphite, 5.6 g (0.06 moles) of triethylamine and 1.05 g (0.011 moles) of magnesium chloride were fed. While stirring the resulting mixed solution at 25° C., 120.0 g (1.2 moles) of methyl isobutyl ketone (MIBK) was added thereto in 1 hour. The resulting mixed solution was further stirred for 1 hour at the same temperature (25° C.) to complete the reaction. Thereafter, the mixed solution was washed to remove the low-boiling point portions, as in (synthesis of raw material 2) of Example 1, and thus, the triethylamine and the magnesium chloride was removed from the mixed solution, to obtain 298.8 g of dibutyl(1-hydroxy-1,3-dimethylbutyl)phosphonate (raw material 3).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07728162B2uspto-grants-2010_06