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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50414Generated: October 26, 2026

Hydrochloric Acid → 1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-

https://huagongshe.com/reaction/50414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantM-XyleneHCID 7929—
ReactantCyanuric chlorideHCID 7954—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChlorobenzeneHCID 7964—
Product1,3,5-Triazine, 2-chloro-4,6-bis(2,4-dimethylphenyl)-HCID 71059—
Product2,4,6-Tris(2,4-dimethylphenyl)-1,3,5-triazineHCID 22475988—

Reaction Steps

To a stirring mixture of 1 eq of cyanuric chloride, 3 eq of AlCl3, and 1.9 eq of m-xylene in chlorobenzene, was added 13% (based on the weight of cyanuric chloride) of concentrated HCl at ice-bath temperature. Within 30 min at room temperature, 97% of the cyanuric chloride had reacted, to produce 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine and 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine in a ratio of 96:4; no side products were detected. Further stirring gave 99.5% cyanuric chloride conversion, with the 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 unchanged and no other products were detected. Thereafter, the reaction mixture was allowed to react with 1.1 eq of resorcinol at 85° C. for 1.5 h. HPLC analysis of the reaction mixture showed the formation of 92.7% 2-(2,4-dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine, 5% 2,4,6-tris(2,4-dimethylphenyl)-1,3,5-triazine, and 2.3% unreacted 2-chloro-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710177B2
Source datasetuspto-grants-2004_03
ORD IDord-f67882ff092a4fcc8d68dc3a0bb4530b
Source noteuspto-grants-2004_03