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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275916Generated: October 31, 2026

2-Chloro-4,6-diphenyl-1,3,5-triazine → 5-(4,6-Diphenyl-1,3,5-triazin-2-yl)-7,7-dimethyl-5,7-dihydroindeno[2,1-b]carbazole

https://huagongshe.com/reaction/2275916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,6-diphenyl-1,3,5-triazineHCID 19698—
ReactantSodium hydrideHCID 24758—
Reactant7,7-Dimethyl-5,7-dihydroindeno[2,1-b]carbazoleHCID 66585204—
SolventDimethylformamideHCID 6228—
Product5-(4,6-Diphenyl-1,3,5-triazin-2-yl)-7,7-dimethyl-5,7-dihydroindeno[2,1-b]carbazoleHCID 66585242—

Reaction Steps

8 g (28.2 mmol) of 12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene are dissolved in 225 ml of dimethylformamide under a protective-gas atmosphere, and 1.5 g of NaH, 60% in mineral oil (37.5 mmol), are added. After 1 h at room temperature, a solution of 2-chloro-4,6-diphenyl-1,3,5-triazine (8.5 g, 31.75 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 12 g (23 mmol, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126970B2
Source datasetuspto-grants-2015_09
ORD IDord-e6406c0fa0f94573bfc04b816a201e57
Source noteuspto-grants-2015_09