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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275930Generated: October 31, 2026

Sodium hydride → 10-(4,6-Bis[1,1';3',1'']terphenyl-5'-yl-1,3,5-triazin-2-yl)-12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene

https://huagongshe.com/reaction/2275930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,4-Di([1,1':3',1''-terphenyl]-5'-yl)-6-chloro-1,3,5-triazineHCID 58299119—
Reactant7,7-Dimethyl-5,7-dihydroindeno[2,1-b]carbazoleHCID 66585204—
SolventDimethylformamideHCID 6228—
Product10-(4,6-Bis[1,1';3',1'']terphenyl-5'-yl-1,3,5-triazin-2-yl)-12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797870—

Reaction Steps

11.3 g (40 mmol) of 12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]-fluorene are dissolved in 285 ml of dimethylformamide under a protective-gas atmosphere, and 1.9 g of 60% NaH in mineral oil (19 mmol) are added. After 1 h at room temperature, a solution of 2-chloro-4,6-bis-[1,1′;3′,1″]terphenyl-5′-yl-1,3,5-triazine (25.1 g, 44 mmol) in 315 ml of dimethylformamide is added dropwise. The reaction mixture is 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 23 g (28 mmol, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126970B2
Source datasetuspto-grants-2015_09
ORD IDord-95855c69c19f42c99ebb511f4ab626fa
Source noteuspto-grants-2015_09