Reacción #1470435

ord-5c2e8e0b4c194bfb87376bfe213cfd0a

Ecuación de reacción

CCCCOP(=O)(Cl)OCCCC
di-n-butyl chlorophosphate
ClCCl
dichloromethane
CC(C)CO
Isobutanol
CCCCOP(=O)(OCCCC)OCC(C)C
di-n-butyl isobutyl phosphate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe pyridinium hydrochloride was filtered off
  2. 2
    Lavadothe solution was washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (25×250 mL)
  3. 3
    SecadoThe organic phase was dried over anhydrous magnesium sulfate for 12 hours
  4. 4
    FiltraciónFiltration of the drying agent
  5. 5
    Otrofollowed by the removal of the solvent

Procedimiento

A solution of di-n-butyl chlorophosphate (130.3 g, 0.57 mole) in 600 mL of dichloromethane containing 55.37 g (0.70 mole) of pyridine was cooled to 0° C. Isobutanol (42.25 g, 0.57 mole) was added dropwise over 1 hour. The formation of a white precipitate was immediately observed. The reaction mixture was then stirred for 24 hours at room temperature. The pyridinium hydrochloride was filtered off, and the solution was washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (25×250 mL). The organic phase was dried over anhydrous magnesium sulfate for 12 hours. Filtration of the drying agent, followed by the removal of the solvent using a Roto-vap, yielded di-n-butyl isobutyl phosphate as a clear colorless liquid. Distillation of the crude product (68° C. at 0.02 torr) gave 125 g of 94.8% di-n-butyl isobutyl phosphate (DBIBP).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06254799B1uspto-grants-2001_07