Reaktion #215413

ord-202fc56c130343d9bcce6157dc42da0f

Reaktionsgleichung

CCCCNc1nc(C)co1
2-butylamino-4-methyloxazole
CCCCCCN=C=O
hexyl isocyanate
CCCCCCNC(=O)N(CCCC)c1nc(C)co1
product
CCCCCCNC(=O)N(CCCC)c1nc(C)co1
1-Butyl-3-hexyl-1-(4-methyl-2-oxazolyl)urea

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux for 3 hours
  2. 2
    SonstigeThe solution was evaporated
  3. 3
    workup.DISSOLUTIONthe residual oil dissolved in ether
  4. 4
    Waschenwashed with dilute HCl
  5. 5
    Sonstigedried
  6. 6
    Sonstigere-evaporated
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in petroleum spirit (40°-60° C.) carbon
  8. 8
    workup.ADDITIONtreated
  9. 9
    Sonstigere-evaporated under vacuum

Vorschrift

A solution of 2-butylamino-4-methyloxazole (10.0 g, 0.065 mol) and hexyl isocyanate (8.25 g, 0.065 mol) in dry benzene was heated under reflux for 3 hours. The solution was evaporated and the residual oil dissolved in ether, washed with dilute HCl, dried and re-evaporated. The residue was dissolved in petroleum spirit (40°-60° C.) carbon treated and re-evaporated under vacuum to give the pure product as a pale oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04259343uspto-grants-1981_03