Reaktion #2045024

ord-a6d4438581c745d39ce56654cb37cb63

Reaktionsgleichung

COC(=O)CCCCCOc1ccc(N)cc1
6-(4-amino-phenoxy)hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(N)cc1
6-(4-Amino-phenoxy)-hexanoic acid methyl ester
CCN(CC)CC
triethylamine
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
COC(=O)CCCCCOc1ccc(N=C=O)cc1
36
Ausbeute 72.3%
COC(=O)CCCCCOc1ccc(N=C=O)cc1
6-(4-Isocyanato-phenoxy)-hexanoic acid methyl ester
Ausbeute 72.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigerose to 60° C
  2. 2
    Temperaturmaintained at this temperature for 26 hours
  3. 3
    TemperaturThe reaction mixture was cooled to room temperature
  4. 4
    Filtrationthe solids were filtered
  5. 5
    workup.DISTILLATIONthe toluene was distilled off under vacuum
  6. 6
    Sonstigeto get crude 36, which
  7. 7
    workup.DISTILLATIONdistilled

Vorschrift

To a mixture of 6-(4-amino-phenoxy)hexanoic acid methyl ester 21 (26 grams, 109.7 mmol) and triethylamine (29.2 g, 288.56 mmol) in toluene (390 ml) under nitrogen atm. was added triphosgene (15.6 grams, 52.56 mmol) in one lot. The reaction was exothermic and the internal temperature rose to 60° 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 cooled to room temperature, the solids were filtered, and the toluene was distilled off under vacuum to get crude 36, which was vacuum distilled to get pure 36 (10 g, 34.7%). M.p: 47-50° C.

Quelle

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