Reaction #1470436

ord-42115002b23c47818f7540bc410a3b19

Reaction equation

CC(C)COP(=O)(Cl)OCC(C)C
diisobutyl chlorophosphate
c1ccncc1
pyridine
CCCCO
n-Butanol
CCCCOP(=O)(OCC(C)C)OCC(C)C
n-butyl diisobutyl phosphate

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONwas added dropwise over 1 hour
  2. 2
    FiltrationThe pyridinium hydrochloride was filtered off
  3. 3
    Washthe solution washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (2×250 mL)
  4. 4
    DryingThe organic phase was dried over anhydrous magnesium sulfate for 12 hours
  5. 5
    FiltrationFiltration of the drying agent
  6. 6
    Otherfollowed by the removal of the solvent

Procedure

A solution of diisobutyl chlorophosphate (130.3 g, 0.57 mole) in 600 mL of dichloromethane and 55.37 g (0.70 mole) of pyridine was cooled to 0° C. n-Butanol (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 washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (2×250 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 n-butyl diisobutyl phosphate as a clear colorless liquid. Distillation of the crude product (68° C. at 0.02 torr) gave 125 g of 96% n-butyl diisobutyl phosphate (BDIBP).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06254799B1uspto-grants-2001_07