Reaction #2045043

ord-b27b6fa33df1451d924b29ee26134380

Reaction equation

CC(Oc1ccc(N)cc1)C(=O)OCCOC(=O)COc1ccc(N)cc1
2-(4-Aminophenoxy)propionic acid-2-[2-(4-aminophenoxy)acetoxy]ethyl ester
C1COCCO1
dioxane
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
C1COCCO1
dioxane
CC(Oc1ccc(N=C=O)cc1)C(=O)OCCOC(=O)COc1ccc(N=C=O)cc1
57
Yield 37.2%
CC(Oc1ccc(N=C=O)cc1)C(=O)OCCOC(=O)COc1ccc(N=C=O)cc1
2-(4-Isocyanatophenoxy)propionic acid-2-[2-(4-isocyanatophenoxy)acetoxy]ethyl ester
Yield 37.2%

Conditions

Temperature
77.5°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureand cooled below 20° C
  2. 2
    Temperaturemaintained for 3 hrs
  3. 3
    workup.DISTILLATIONThe condenser was arranged for distillation and solvent
  4. 4
    Otherremoved by distillation at one atm. until the volume of the reaction mixture
  5. 5
    workup.ADDITIONFresh dry dioxane (50 ml) was added
  6. 6
    workup.DISTILLATIONsolvents distilled off under vacuum
  7. 7
    OtherThe residue was re-evaporated twice from dry dioxane

Procedure

2-(4-Aminophenoxy)propionic acid-2-[2-(4-aminophenoxy)acetoxy]ethyl ester 56 (5.2 g, 13.9 mmol) was dissolved in dry dioxane (80 ml) under nitrogen atm. and cooled below 20° C. A solution of triphosgene (7 g, 23.6 mmol) in dry dioxane (20 ml) was added dropwise. The mixture was heated slowly to 75-80° C. and maintained for 3 hrs. The condenser was arranged for distillation and solvent removed by distillation at one atm. until the volume of the reaction mixture was reduced to approx. one third. Fresh dry dioxane (50 ml) was added and solvents distilled off under vacuum. The residue was re-evaporated twice from dry dioxane to give 57 (2.2 g, 37.2%) as a light yellow syrup.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08409559B2uspto-grants-2013_04