Reaktion #78696

ord-a6adafa98b074b1a86687059c1c36a2f

Reaktionsgleichung

Clc1nc(Cl)nc(Cl)n1
cyanuric chloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
Cc1cccc(C)c1
m-xylene
[Al+3].[OH-].[OH-].[OH-]
aluminum hydroxide
Clc1nc(Cl)nc(Cl)n1
cyanuric chloride
Ausbeute 98.0%
Cc1ccc(-c2nc(Cl)nc(-c3ccc(C)cc3C)n2)c(C)c1
2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine
Cc1ccc(-c2nc(-c3ccc(C)cc3C)nc(-c3ccc(C)cc3C)n2)c(C)c1
2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe cooling bath was removed after 10 min
  2. 2
    workup.STIRRINGthe reaction mixture stirred at room temperature
  3. 3
    workup.WAITHPLC analysis after 20 h at room temperature showed

Vorschrift

To a stirring mixture of 3.7 g (1 eq) of cyanuric chloride, 8 g (3 eq) of aluminum chloride in 50 mL chlorobenzene was added 0.39 g (0.5 eq) of aluminum hydroxide at ice-bath temperature. After 10 min of stirring, 1.9 eq of m-xylene was added. The cooling bath was removed after 10 min and the reaction mixture stirred at room temperature. HPLC analysis after 20 h at room temperature showed 98% of cyanuric chloride conversion to 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine and 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine, formed in a ratio of 80:20.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06710177B2uspto-grants-2004_03