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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627748Generated: October 31, 2026

2-Chloro-4,6-diphenyl-1,3,5-triazine → 6-(4,6-Diphenyl-1,3,5-triazin-2-yl)-8,8-dimethyl-8H-indolo[3,2,1-de]acridine

https://huagongshe.com/reaction/1627748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,6-diphenyl-1,3,5-triazineHCID 19698—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant8,8-Dimethyl-8H-indolo[3,2,1-de]acridine-6-boronic acidHCID 67326198—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product6-(4,6-Diphenyl-1,3,5-triazin-2-yl)-8,8-dimethyl-8H-indolo[3,2,1-de]acridineHCID 68014513—

Reaction Steps

36 g (110.0 mmol) of 8,8-dimethyl-8H-indolo[3,2,1-de]acridine-6-boronic acid, 29.5 g (110.0 mmol) of 2-chloro-4,6-diphenyl-1,3,5-triazine and 44.6 g (210.0 mmol) of tripotassium phosphate are suspended in 500 ml of toluene, 500 ml of dioxane and 500 ml of water. 913 mg (3.0 mmol) of tri-o-tolylphosphine and then 112 mg (0.5 mmol) of palladium (II) acetate are added to this suspension, and the reaction mixture is heated under reflux for 16 h. After cooling, the organic phase is separated off, filtered through silica gel, washed three times with 200 ml of water and subsequently evaporated to dryness. The residue is recrystallised from toluene and from dichloromethane/isopropanol and finally sublimed in a high vacuum, the purity is 99.9%. The yield is 46 g (89 mmol), corresponding to 83% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785636B2
Source datasetuspto-grants-2014_07
ORD IDord-a6770a7d366e4c6b95e63f56fa609ed3
Source noteuspto-grants-2014_07