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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325752Generated: October 25, 2026

Cyanuric chloride → 2,4-Bis(4-ethynylphenyl)-6-phenyl-1,3,5-triazine

https://huagongshe.com/reaction/325752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant(4-Bromophenylethynyl)trimethylsilaneHCID 4226980—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product2,4-Bis(4-ethynylphenyl)-6-phenyl-1,3,5-triazineHCID 20429680—

Reaction Conditions

Temperature60 °C

Reaction Steps

One mole of cyanuric chloride was treated with one mole of phenylmagnesium bromide as described in Step I of Example I. The product of this reaction (2.3 g, 0.01 mole) in 25 ml of tetrahydrofuran (THF) was added slowly to a refluxing solution of the Grignard reagent prepared from 1-(trimethylsilyl)-2-(4-bromophenyl)acetylene (0.03 moles) and magnesium (0.75 g). The solution was stirred overnight, filtered, and the solvent removed. To the residue which remained was added a solution of KOH (10.0 g) in water (5 ml), anhydrous ethanol (100 ml) and dioxane (100 ml). The resulting mixture was heated for 2.5 hours at 60° C., filtered, and the solvent removed. Chromatographic separation of the resulting residue yielded a yellow solid, 6-phenyl-2,4-bis(4-ethynylphenyl)-s-triazine, which melted at approximately 215° C. with rapid polymerization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442278
Source datasetuspto-grants-1984_04
ORD IDord-4bf43c85562b43df8b7424e0a6d50c11
Source noteuspto-grants-1984_04