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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Phenol, tribromo- | HCID 32928 | — |
| Reactant | Tribromophenolate | HCID 18781512 | — |
| Product | 2,4,6-Tris(2,3,4-tribromophenoxy)-1,3,5-triazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06075142 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-9436138d427a430c88d9c07625c9c5ba |
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| Source note | uspto-grants-2000_06 |
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