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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50417Erstellt: 24. Oktober 2026

M-Xylene → Cyanuric chloride

https://huagongshe.com/de/reaction/50417

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktM-XyleneHCID 7929—
EduktCyanuric chlorideHCID 7954—
EduktSodium HydroxideHCID 14798—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelChlorobenzeneHCID 7964—
ProduktCyanuric chlorideHCID 795491%
Produkt1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-HCID 71059—
Produkt2,4,6-Tris(2,4-dimethylphenyl)-1,3,5-triazineHCID 22475988—

Reaktionsschritte

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 0.4 mL of aqueous sodium hydroxide solution (50%) at ice-bath temperature. After 10 min of stirring, 1.9 eq of m-xylene was added. The cooling bath was removed and the reaction mixture stirred at room temperature. HPLC analysis after 30 min at room temperature showed 91% 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 96:4. A second sample analyzed after 1 h at room temperature showed 94% of cyanuric chloride conversion to 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine and 2,4,6-tris(2,4-dimethylpheny)-1,3,5-triazine, in a ratio of 92:8. After a total of 4 h at room temperature, HPLC analysis showed 95% conversion of cyanuric chloride and a ratio of 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine to 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine of 89:11.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710177B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-1f71922308694f0491db17661ae24514
Quellennotizuspto-grants-2004_03