HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019300Generated: October 31, 2026
Benzene → 2-Chloro-4,6-diphenyl-1,3,5-triazine
https://huagongshe.com/reaction/1019300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 2-Chloro-4,6-diphenyl-1,3,5-triazine | HCID 19698 | — |
Reaction Steps
To a stirring mixture of 1 eq of cyanuric chloride and 3 eq of aluminum chloride in o-dichlorobenzene at ice bath temperature was added concentrated HCl (13 wt % based on cyanuric chloride). After 10 minutes, 1.95 eq of benzene was added and the reaction mixture stirred at ice bath temperature for 10 minutes. The cooling bath was removed, the reaction was allowed to warm to room temperature, and stirred. After 26 h at room temperature, an HPLC analysis indicated about 86% cyanuric chloride conversion to 2-chloro-2,6-bisphenyl-1,3,5-triazine. The stirring was continued for 24 h at room temperature. The HPLC analysis showed the cyanuric chloride conversion to 92% with >96% being 2-chloro-4,6-bisphenyl-1,3,5-triazine and less than 2% of 2,4,6-trisphenyl-1,3,5-triazine. The result was confirmed by LCMS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486316B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-56a8208b8ca04937a5ddfd1f97a68c50 |
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| Source note | uspto-grants-2002_11 |
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