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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325753Generated: October 31, 2026

Cyanuric chloride → HCID 20429677, compound

https://huagongshe.com/reaction/325753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 20429677HCID 20429677—

Reaction Steps

One mole of cyanuric chloride was treated with phenylmagnesium bromide as described in Step I of Example I. The resulting reaction product (10.0 g, 0.044 mole) in CHCl3 (100 ml) was stirred in a 250 ml 3-neck round bottom flask while m-aminophenylacetylene (10.5 g, 0.09 mole) was added dropwise with cooling. To this mixture was added K2CO3 (12.4 g, 0.09 mole) and water (20 ml). The organic layer was separated, dried, and the solvent evaporated. The residue was triturated in benzene and dried to give 6-phenyl-2,4-bis(3-ethynylphenylamino)-s-triazine a compound that melted at 210° C. with polymerization. Thermo-gravimetric analysis showed that the polymer was stable to 425° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442278
Source datasetuspto-grants-1984_04
ORD IDord-865361605b6b473b97436e5841037f59
Source noteuspto-grants-1984_04