Reaktion #54195

ord-31cafcba60664a8b99c5337a02869b22

Reaktionsgleichung

N#CCCN(CCO)c1ccccc1
N-(2-cyanoethyl)-N-(2-hydroxyethyl)aniline
N#C[O-].[K+]
potassium cyanate
O=S1(=O)CCCC1
sulfolane
O=S1(=O)CCCC1
sulfolane
CCCBr
1-bromopropane
CCCNC(=O)OCCN(CCC#N)c1ccccc1
N-(2-cyanoethyl)-N-[2-(N-propylcarbamoyloxy)ethyl]aniline

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONTo a mixture of 4 g
  2. 2
    workup.STIRRINGThe resulting mixture is stirred at 90°-100° C. for three hours
  3. 3
    Sonstigethe resulting layers separated

Vorschrift

To a mixture of 4 g. (.05 mole) of potassium cyanate and 25 ml. of sulfolane at 90° C. are added dropwise 9 ml. (12.3 g, 0.1 mole) of 1-bromopropane over a one-hour period. After 10 minutes of stirring at the same temperature, a solution of 6 g. (0.027 mole) of N-(2-cyanoethyl)-N-(2-hydroxyethyl)aniline in 5 ml. sulfolane is added. The resulting mixture is stirred at 90°-100° C. for three hours and then allowed to cool to 50° C. The mixture is poured into 1 liter of water under agitation, and the resulting layers separated. TLC of the organic layer in 4:1 benzene: acetone shows the absence of starting alcohol with the product of the above formula.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04147716uspto-grants-1979_04