HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50413Erstellt: 23. Oktober 2026
Resorcinol → 1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-
https://huagongshe.com/de/reaction/50413
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Resorcinol | HCID 5054 | — |
| Edukt | M-Xylene | HCID 7929 | — |
| Edukt | Cyanuric chloride | HCID 7954 | — |
| Edukt | 1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)- | HCID 71059 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)- | HCID 71059 | — |
| Produkt | 2,4,6-Tris(2,4-dimethylphenyl)-1,3,5-triazine | HCID 22475988 | — |
Reaktionsschritte
Cyanuric chloride was allowed to react with 2.05 eq of m-xylene, in the presence of 3 eq of AlCl3 and 0.2 of resorcinol, in chlorobenzene at 5° C. for 0.5 h and then at room temperature for 3 h. The first step (conversion to 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine) was completed in less than 16 h, with more than 98% cyanuric chloride conversion as determined by HPLC analysis. 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine and 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine were formed in an 86:14 ratio; no other products were detected. The reaction mixture was allowed to react with additional resorcinol at 110° C. for 1.5 h. HPLC analysis showed a product mixture of 82% 2-(2,4-dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine, 14% 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine, and 2% 2,4,6-tris(2,4-dihydroxyphenyl)-1,3,5-triazine, with only 1.5% unreacted 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06710177B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-a98db76593b44ef79acd4d9ab98eb4ff |
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| Quellennotiz | uspto-grants-2004_03 |
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