Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634552Generated: October 26, 2026

Potassium Carbonate → 7-[3-(4,6-Diphenylpyrimidin-2-yl)phenyl]-12,12-dimethyl-10-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene

https://huagongshe.com/reaction/634552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Bromophenyl)-4,6-diphenylpyrimidineHCID 58943181—
Reactant7-Borono12,12-dimethyl-10-phenyl-10,12-dihydro-10-aza-indeno[2,1-b]fluoreneHCID 86696086—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product7-[3-(4,6-Diphenylpyrimidin-2-yl)phenyl]-12,12-dimethyl-10-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 86696087—

Reaction Conditions

Temperature80 °C

Reaction Steps

16 g (43.3 mmol) of 2-(3-bromophenyl)-4,6-diphenylpyrimidine 14 and 19.3 g (48 mmol) of 7-borono12,12-dimethyl-10-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene 13 are dissolved in 80 ml of toluene and degassed. 281 ml of a degassed 2M K2CO3 and 2.5 g (2.2 mmol) of Pd(OAc)2 are added. The reaction mixture is subsequently stirred for 48 h at 80° C. under a protective-gas atmosphere. Additional toluene is added to the cooled solution, which is washed a number of times with water, dried and evaporated. The product is purified by column chromatography on silica gel with toluene/heptane (1:2). The purity is 99.9%. Yield: 22 g (31 mmol), 77% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09324954B2
Source datasetuspto-grants-2016_04
ORD IDord-8c632538039846adae8d95f356cb842c
Source noteuspto-grants-2016_04