Reaktion #573515

ord-ff9408c4f1f64d81bc2b440859e6597b

Reaktionsgleichung

NC(N)=O
urea
CCCCCCCCOc1ccc(C(=O)O)cc1
p-(n-octyloxy)benzoic acid
NC(N)=O
urea
[Na+].[OH-]
sodium hydroxide
CCCCCCCCOc1ccc(C(=O)NC(N)=O)cc1
p-(n-octyloxy)benzoylurea

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONA 500 ml 3-neck round bottom flask containing a magnetic stirrer
  2. 2
    TemperaturThe mixture is heated to 120 deg C
  3. 3
    Temperaturcooled
  4. 4
    Sonstigeprecipitates the product
  5. 5
    Sonstigewhich is isolated by filtration
  6. 6
    workup.ADDITIONrespectively) in addition to the conspicuous absence of any absorbance at 3490 cm-1 (acid O--H stretching)

Vorschrift

A 500 ml 3-neck round bottom flask containing a magnetic stirrer, thermometer, and a reflux condensor with a gas egress tube for a nitrogen blanket is charged with a one part apiece of p-(n-octyloxy)benzoic acid and urea dissolved in 15 parts N-methylpyrrolidone containing 0.01wt percent triphenylphosphite. The mixture is heated to 120 deg C. for approximately 2-5 hours and then cooled. The addition of a copious amount of 3M aqueous sodium hydroxide to a cooled solution precipitates the product, which is isolated by filtration. Infrared absorbance at 3250 cm-1 (urea N--H stretching) and at 1705 cm-1 and 1640 cm-1 (amide and urea C=O stretching, respectively) in addition to the conspicuous absence of any absorbance at 3490 cm-1 (acid O--H stretching) confirm the chemical transformation.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05292351uspto-grants-1994_03