Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421357Generated: October 26, 2026

Chloride → 2,4,6-Tris(2,3,4-tribromophenoxy)-1,3,5-triazine

https://huagongshe.com/reaction/1421357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantCyanuric chlorideHCID 7954—
ReactantPhenol, tribromo-HCID 32928—
ReactantTribromophenolateHCID 18781512—
Product2,4,6-Tris(2,3,4-tribromophenoxy)-1,3,5-triazineHCID 23496457—

Reaction Steps

An exemplary production process according to this invention comprises preparing an aqueous tribromophenolate solution and dripping this aqueous solution to a dispersion or solution of cyanuric chloride and tertiary amine in a non-hydrophilic solvent or adding said tertiary amine and a powder of cyanuric chloride to said aqueous solution. The preferred molar ratio of cyanuric chloride to tribromophenol is 1:2.94-3.60. Where both a tertiary amine and a phase transfer catalyst are employed, an exemplary procedure comprises preparing an aqueous tribromophenolate solution, adding a tertiary amine thereto and dripping the mixture to a solution or dispersion of cyarnuric chloride and phase transfer catalyst in a non-hydrophilic solvent or adding said phase transfer catalyst, said tertiary amine and a powder of cyanuric chloride to the aqueous tribromophenolate solution. After the above dripping or addition, the reaction system is aged where necessary and the non-hydrophilic solvent is removed from the reaction system at atmospheric or subatmospheric pressure. In this manner, tris(tribromophenoxy)-s-triazine of high purity can be obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06075142
Source datasetuspto-grants-2000_06
ORD IDord-9436138d427a430c88d9c07625c9c5ba
Source noteuspto-grants-2000_06