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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773059Generated: November 2, 2026

Toluene → HCID 131734703, compound

https://huagongshe.com/reaction/1773059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-1,10-phenanthrolineHCID 355193—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 131734704HCID 131734704—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 131734703HCID 131734703—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a stream of argon, 1.13 g of 2-chloro-1,10-phenanthroline, 1.57 g of 2,4-di(3-biphenylyl-6-[3,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1,3,5-triazine, 280 mg of lithium chloride and 203 mg of tetrakis(triphenylphosphine)palladium were suspended in a toluene (60 mL)/ethanol (15 mL) mixed solvent. 8.8 mL of a 2.0 M aqueous sodium carbonate solution was added in the obtained suspension, and the mixture was stirred at 100° C. for 65 hours. Then the reaction mixture was left to be cooled to room temperature, and distilled under a reduced pressure to remove low-boiling point ingredients. The thus-obtained residue was purified by alumina column chromatography using chloroform as a developing solvent to give 1.22 g of target 2,4-di(3-biphenylyl-6-[3,5-bis(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine as a white powder (yield, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09252368B2
Source datasetuspto-grants-2016_02
ORD IDord-a647b43b884e43588fceaa35edfa4ea2
Source noteuspto-grants-2016_02