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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019303Generated: November 2, 2026

Hydrochloric Acid → 2,4-Bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine (This product is only available in Japan.)

https://huagongshe.com/reaction/1019303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-ButylbenzeneHCID 7366—
ReactantCyanuric chlorideHCID 7954—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichlorobenzeneHCID 7239—
Product2,4-Bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine (This product is only available in Japan.)HCID 22475991—

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 tert-butylbenzene was added and the reaction was stirred at ice bath temperature for 10 minutes. The cooling bath was removed, the reaction mixture was allowed to warm to room temperature, and stirred. After 2 h, HPLC analysis indicated 62% cyanuric chloride conversion to 2-chloro-4,6-bis(4-tert-butylphenyl)-1,3,5-triazine as the major product (>78%). The reaction mixture was stirred at room temperature for an additional 24 h. HPLC analysis showed 83% cyanuric chloride conversion to 2-chloro-4,6-bis(4-tert-butylphenyl)-1,3,5-triazine as the major product (>72%), with the isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486316B1
Source datasetuspto-grants-2002_11
ORD IDord-1b7cc4f182a349398056b818b5eaed48
Source noteuspto-grants-2002_11