Reaktion #4253

ord-848069fa4f1f477c85839d23e4203cc5

Reaktionsgleichung

CCCCCCCCOC(=O)c1ccc(N)cc1
octyl p-aminobenzoate
Clc1nc(Cl)nc(Cl)n1
cyanuric chloride
Cl
hydrogen chloride
CCCCCCCCOC(=O)c1ccc(NN2CN(Nc3ccc(C(=O)OCCCCCCCC)cc3)CN(Nc3ccc(C(=O)OCCCCCCCC)cc3)C2)cc1
1,3,5-Tris-(p-(oct-1-yloxycarbonyl)-anilino)-s-triazine

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed twice with saturated sodium bicarbonate solution and once with water
  2. 2
    Temperaturcooled to room temperature
  3. 3
    SonstigeThe white crystals precipitated
  4. 4
    Filtrationwere filtered off under suction

Vorschrift

75 g of octyl p-aminobenzoate and 18.5 g of cyanuric chloride in 1,000 ml of xylene were heated at 140° C. for 8 hours. After the evolution of hydrogen chloride was complete, the reaction solution was cooled to 90° C., washed twice with saturated sodium bicarbonate solution and once with water and then cooled to room temperature. The white crystals precipitated were filtered off under suction.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04724137uspto-grants-1988_02