Reaction #81150

ord-d728077f295740f79612ef0dd40891fd

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONwere added
  2. 2
    Temperatureunder cooling with ice
  3. 3
    workup.STIRRINGThe mixture was stirred at room temperature overnight
  4. 4
    OtherThe reaction solution was evaporated under reduced pressure
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
  6. 6
    Washsequentially washed with 1N hydrochloric acid, water
  7. 7
    Dryinga saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate
  8. 8
    OtherThe drying agent was separated by filtration
  9. 9
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure

Procedure

29.2 g of the diethylphosphonoacetic acid thus obtained was dissolved in 350 me of methylene chloride, and 17.8 g of allyl alcohol, 1.92 g of 4-dimethylaminopyridine and 29.0 g of 1-ethyl-3-(3-methylaminopropyl)carbodiimide hydrochloride were added thereto with stirring under cooling with ice. The mixture was stirred at room temperature overnight. The reaction solution was evaporated under reduced pressure. The residue was dissolved in ethyl acetate, then sequentially washed with 1N hydrochloric acid, water, a saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and then the solvent was distilled off under reduced pressure to obtain 28.9 g of allyl diethylphosphonoacetate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05616803uspto-grants-1997_04