Réaction #2045017

ord-0f2a729f371b4e159960c40dbc7d47a9

Équation de réaction

COC(=O)COc1ccc(N)cc1
(4-Amino-phenoxy)-acetic acid methyl ester
CCN(CC)CC
triethylamine
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
COC(=O)COc1ccc(N=C=O)cc1
28
Rendement 159.1%
COC(=O)COc1ccc(N=C=O)cc1
(4-Isocyanato-phenoxy)-acetic acid methyl ester
Rendement 159.1%

Solvants

Conditions de réaction

Température
25°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureLater the reaction mixture was heated to 75° C. over a period of one hour
  2. 2
    Températuremaintained at this temperature for 26 hours
  3. 3
    TempératureThe reaction mixture was then cooled to room temperature
  4. 4
    Filtrationthe solids were filtered off
  5. 5
    workup.DISTILLATIONthe toluene was distilled off under vacuum
  6. 6
    Autreto get crude 28, which
  7. 7
    workup.DISTILLATIONdistilled

Mode opératoire

To a mixture of (4-Amino-phenoxy)-acetic acid methyl ester 15 (15 g, 82.87 mmol) and triethylamine (16.77 g, 165.73 mmol) in toluene (225 ml) under nitrogen atm. at 0° C. was added triphosgene (9 g, 30.33 mmol) in one lot. The reaction was exothermic and the temperature raised to 25° C. Later the reaction mixture was heated to 75° C. over a period of one hour and maintained at this temperature for 26 hours. The reaction mixture was then cooled to room temperature, the solids were filtered off, and the toluene was distilled off under vacuum to get crude 28, which was vacuum distilled to get pure 28 (10 g, 58.3%) as a white powder. M.p: 50-53° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08409559B2uspto-grants-2013_04