Reaktion #725901

ord-b59539cde2824e0da3a3a3758f66be0d

Reaktionsgleichung

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
Ausbeute 159.1%
COC(=O)COc1ccc(N=C=O)cc1
(4-Isocyanato-phenoxy)-acetic acid methyl ester
Ausbeute 159.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturLater the reaction mixture was heated to 75° C. over a period of one hour
  2. 2
    Temperaturmaintained at this temperature for 26 hours
  3. 3
    TemperaturThe 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
    Sonstigeto get crude 28, which
  7. 7
    workup.DISTILLATIONdistilled

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07691364B2uspto-grants-2010_04