Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275925Generated: October 31, 2026

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

https://huagongshe.com/reaction/2275925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,6-diphenyl-1,3,5-triazineHCID 19698—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797789—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-10-(4,6-diphenyl-1,3,5-triazin-2-yl)-12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797951—

Reaction Steps

25.5 g (70.4 mmol) of 7-bromo-12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene are dissolved in 400 ml of dimethylformamide under a protective-gas atmosphere, and 3.1 g of 60% NaH in mineral oil (78 mol) are added. After 1 h at room temperature, a solution of 2-chloro-4,6-diphenyl-1,3,5-triazine (22.6 g, 84.5 mmol) in 100 ml of THF 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 recrystallised from toluene. Yield: 40 g (67 mmol), 95% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126970B2
Source datasetuspto-grants-2015_09
ORD IDord-335c300690054a5c991c04d55e1a3423
Source noteuspto-grants-2015_09