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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275919Generated: October 31, 2026

2-Chloro-4,6-diphenyl-1,3,5-triazine → 10-(4,6-Diphenyl-1,3,5-triazin-2-yl)-12,12-dimethyl-7-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene

https://huagongshe.com/reaction/2275919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,6-diphenyl-1,3,5-triazineHCID 19698—
ReactantSodium hydrideHCID 24758—
Reactant12,12-Dimethyl-7-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797462—
SolventDimethylformamideHCID 6228—
Product10-(4,6-Diphenyl-1,3,5-triazin-2-yl)-12,12-dimethyl-7-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797596—

Reaction Steps

10 g (27.7 mmol) of 12,12-dimethyl-7-phenyl-10,12-dihydro-10-azaindeno-[2,1-b]fluorene are dissolved in 275 ml of dimethylformamide under a protective-gas atmosphere, and 1.45 g of NaH, 60% in mineral oil (36 mmol), are added. After 1 h at room temperature, a solution of 2-chloro-4,6-diphenyl-1,3,5-triazine (8.2 g, 30.5 mmol) in 75 ml of dimethylformamide is added dropwise. The reaction mixture is then stirred at room temperature for 12 h. After this time, the reaction mixture is poured onto ice and extracted three times with dichloromethane. The combined organic phases are dried over Na2SO4 and evaporated. The residue is extracted with hot toluene. The yield is 14.7 g (24.9 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126970B2
Source datasetuspto-grants-2015_09
ORD IDord-48697e7d96a14110af314f3d1d8dea3e
Source noteuspto-grants-2015_09