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HRID 50412Erstellt: 24. Oktober 2026
M-Xylene → 2,4-Dichloro-6-(2,4-dimethylphenyl)-1,3,5-triazine
https://huagongshe.com/de/reaction/50412
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | M-Xylene | HCID 7929 | — |
| Edukt | Cyanuric chloride | HCID 7954 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 2,4-Dichloro-6-(2,4-dimethylphenyl)-1,3,5-triazine | HCID 11402553 | — |
Reaktionsschritte
Cyanuric chloride (1.84 g) was allowed to react with 1.9 eq of m-xylene and 2.5 eq (3.35 g) of AlCl3 in 25 mL of chlorobenzene at 5° C. for 0.5 h and then at room temperature for 3 h. Analysis by HPLC, after 2.5 h, showed that less than 8% of cyanuric chloride had reacted to form only 2,4-dichloro-6-(2,4-dimethylphenyl)-1,3,5-triazine, no 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine or 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine were present. The reaction was allowed to continue at room temperature. After 24 hours, HPLC analysis showed about 51% cyanuric chloride conversion and formation of 2,4-dichloro-6-(2,4-dimethylphenyl)-1,3,5-triazine and 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine in the ratio of 95:5, respectively. No 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine was detected.
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-fa9ccb0d66fe4110b5d1c310a716d5d0 |
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| Quellennotiz | uspto-grants-2004_03 |
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